1. Home
  2. List

Narrow By

  More
Search Options

17 records – page 1 of 1.

Urea cycle disorders: A guide for patients, parents and families

https://libraries.phsa.ca/permalink/catalog113941

http://www.nucdf.org/documents/UCD_Guide_NewFamilies_USA.pdf

National Urea Cycle Disorders Foundation. Pasadena, CA: National Urea Cycle Disorders Foundation , 2015. (Online, Pamphlet)
Audience
Patient or Public
Agency
BC Children's and Women's
URL Notes
Click on the link above to view/print.
You or your child have/has been diagnosed with a urea cycle disorder. Initially any information regarding these types of condition is hard to understand, especially at a time when you are naturally very worried and suddenly provided with lots of medical information. By describing this condition in …
Title
Urea cycle disorders: A guide for patients, parents and families
Corporate Author
National Urea Cycle Disorders Foundation
Place
Pasadena, CA
Publisher
National Urea Cycle Disorders Foundation
Year Published
2015
Topics
Genetic Disorders
Urinary System
Abstract
You or your child have/has been diagnosed with a urea cycle disorder. Initially any information regarding these types of condition is hard to understand, especially at a time when you are naturally very worried and suddenly provided with lots of medical information. By describing this condition in booklet format, you will be able to read it at your leisure, and then write down any important questions that you may want to ask your specialist doctor, nurse or dietitian.
Language
English
Material Type
Online
Pamphlet
Agency
BC Children's and Women's
URL
http://www.nucdf.org/documents/UCD_Guide_NewFamilies_USA.pdf
URL Notes
Click on the link above to view/print.
Audience
Patient or Public

Factor V Leiden: Information for patient and families

https://libraries.phsa.ca/permalink/catalog112230

http://www.cw.bc.ca/library/PDF/pamphlets/BCCH1634_FactorVLeiden-2012_July.pdf

Hematology Department. Vancouver, BC: BC Children's Hospital , 2012. (Pamphlet)
Audience
Patient or Public
Agency
BC Children's and Women's
Call Number
BCCH1634
URL Notes
Click on the link above to view/print.
This pamphlet provides information about the blood clotting disorder Factor V Leiden, including how it affects clotting; how the diagnosis is made; information about the genetic inheritance; treatment information; and tips for what you can do if you have Factor V Leiden.
Title
Factor V Leiden: Information for patient and families
Corporate Author
Hematology Department
Place
Vancouver, BC
Publisher
BC Children's Hospital
Year Published
2012
Physical Description
PDF file: 6 p.
Topics
Genetic Disorders
Abstract
This pamphlet provides information about the blood clotting disorder Factor V Leiden, including how it affects clotting; how the diagnosis is made; information about the genetic inheritance; treatment information; and tips for what you can do if you have Factor V Leiden.
Language
English
Material Type
Pamphlet
Agency
BC Children's and Women's
URL
http://www.cw.bc.ca/library/PDF/pamphlets/BCCH1634_FactorVLeiden-2012_July.pdf
URL Notes
Click on the link above to view/print.
Audience
Patient or Public
Call Number
BCCH1634

VHL handbook: What you need to know about VHL: A reference handbook for people with von Hippel-Lindau Disease, their families, and support personnel

https://libraries.phsa.ca/permalink/catalog106207

http://www.vhl.org/handbook/hbcopy.htm

VHL Family Alliance (Eds.). VHL Family Alliance , 2005. Version 3.0. (Book) — 1 copy, 1 available
Audience
Patient or Public
Agency
BC Children's and Women's
Location
Family Support & Resource Centre
Call Number
GI 300 WHA 2005
URL Notes
Click on the link above to view as a PDF file (2137K). Also available in Spanish from the same website.
This handbook is compiled by the VHL Family Alliance. It covers the impact of Von Hippel-Lindau (VHL)disease on all aspects of life, including definitions and treatment options.
Title
VHL handbook: What you need to know about VHL: A reference handbook for people with von Hippel-Lindau Disease, their families, and support personnel
Corporate Author
VHL Family Alliance (Eds.)
Edition
Version 3.0
Publisher
VHL Family Alliance
Year Published
2005
Physical Description
50 p.
Topics
Genetic Disorders
Chromosome Abnormalities
Abstract
This handbook is compiled by the VHL Family Alliance. It covers the impact of Von Hippel-Lindau (VHL)disease on all aspects of life, including definitions and treatment options.
ISBN
1929539002
Language
English
Material Type
Book
Agency
BC Children's and Women's
Location
Family Support & Resource Centre
URL
http://www.vhl.org/handbook/hbcopy.htm
URL Notes
Click on the link above to view as a PDF file (2137K). Also available in Spanish from the same website.
Audience
Patient or Public
Call Number
GI 300 WHA 2005
Copy 1 BC Children's and Women's Family Support & Resource Centre Available
thumbnail
Lewis, Vicky. Malden, MA: Blackwell Publishing , 2003. 2nd ed. (Book) — 1 copy, 1 available
Audience
Patient or Public
Agency
BC Children's and Women's
Location
Sunny Hill Education Resource Centre
Call Number
GK 300 LEW 2003
Reviews research on the development of blind children, deaf children, and children with spina bifida, cerebral palsy, Down's syndrome and autism. Includes research on children with developmental co-ordination disorder. Provides information on the nature of each disability, assessment, incidence, an…
Title
Development and disability
Author
Lewis, Vicky
Edition
2nd ed.
Place
Malden, MA
Publisher
Blackwell Publishing
Year Published
2003
Physical Description
Paperback, 23 cm x 15 cm, 454 p.
Topics
Child Development
Developmental Disability
Genetic Disorders
Physical Disability. Physically Challenged
Abstract
Reviews research on the development of blind children, deaf children, and children with spina bifida, cerebral palsy, Down's syndrome and autism. Includes research on children with developmental co-ordination disorder. Provides information on the nature of each disability, assessment, incidence, and causal factors. Summarizes the effect of each disability on the development of motor skills, perception, cognition, communication, emotion and social skills.
ISBN
978-0-631-23466-1
Language
English
Material Type
Book
Agency
BC Children's and Women's
Location
Sunny Hill Education Resource Centre
Audience
Patient or Public
Call Number
GK 300 LEW 2003
Copy 1 BC Children's and Women's Sunny Hill Education Resource Centre Redevelopment Available
thumbnail

Genetic disorders and the fetus: Diagnosis, prevention and treatment

https://libraries.phsa.ca/permalink/catalog112671
Milunsky, Aubrey (ed.), Milunsky, Jeff M. (ed.). Hoboken, NJ: Wiley-Blackwell , 2010. 6th ed. (Book) — 1 copy, 1 available
Audience
Professional
Agency
BC Children's and Women's
Location
Study & Learning Commons
Call Number
REF GI 300 MIL 2010
This text is in its 6th edition as a major repository of facts about prenatal diagnosis. It is an essential resource for all engaged in prenatal genetic diagnosis, especially obstetricians, maternal-fetal medicine specialists, medical geneticists, genetic counsellors, and pediatricians.
Title
Genetic disorders and the fetus: Diagnosis, prevention and treatment
Author
Milunsky, Aubrey (ed.)
Milunsky, Jeff M. (ed.)
Edition
6th ed.
Place
Hoboken, NJ
Publisher
Wiley-Blackwell
Year Published
2010
Physical Description
Hardcover: 1135 p.
Topics
Genetic Disorders
Genetics
UBC MD Undergrad
Abstract
This text is in its 6th edition as a major repository of facts about prenatal diagnosis. It is an essential resource for all engaged in prenatal genetic diagnosis, especially obstetricians, maternal-fetal medicine specialists, medical geneticists, genetic counsellors, and pediatricians.
ISBN
9781405190879
Language
English
Material Type
Book
Agency
BC Children's and Women's
Location
Study & Learning Commons
Audience
Professional
Call Number
REF GI 300 MIL 2010
Copy 1 BC Children's and Women's Study & Learning Commons REF Available
thumbnail

Missing genetic pieces: Strategies for living with VCFS, the chromosome 22q11 deletion.

https://libraries.phsa.ca/permalink/catalog108820
Baker-Gomez, Sherry. Phoenix, AZ: Desert Pearl Publishing , c2004. (Book) — 1 copy, 1 available
Audience
Patient or Public
Agency
BC Children's and Women's
Location
Family Support & Resource Centre
Call Number
GI 300 BAK 2004
This is a comprehensive handbook for parents, professionals and anyone wanting to know about chromosome 22 deletion (22q11) and its dynamics. It includes personal stories, dictionary of terms, useful tips and resources.
Title
Missing genetic pieces: Strategies for living with VCFS, the chromosome 22q11 deletion.
Author
Baker-Gomez, Sherry
Place
Phoenix, AZ
Publisher
Desert Pearl Publishing
Year Published
c2004
Physical Description
Paperback; xiv, 559 p.
Topics
Genetic Disorders
Heart/Heart Diseases-Children
Children with Facial Difference
Abstract
This is a comprehensive handbook for parents, professionals and anyone wanting to know about chromosome 22 deletion (22q11) and its dynamics. It includes personal stories, dictionary of terms, useful tips and resources.
ISBN
097453580X
Language
English
Material Type
Book
Agency
BC Children's and Women's
Location
Family Support & Resource Centre
Audience
Patient or Public
Call Number
GI 300 BAK 2004
Copy 1 BC Children's and Women's Family Support & Resource Centre Available
thumbnail

The boy in the moon: A father's search for his disabled son

https://libraries.phsa.ca/permalink/catalog111520
Brown, Ian. Toronto, ON: Vintage Canada , 2010. (Book) — 1 copy, 1 available
Audience
Patient or Public
Agency
BC Children's and Women's
Location
Family Support & Resource Centre
Call Number
GK 655 BRO 2009
This book tells the story of a father's personal journey and search for his disabled son. The author's son was born with a rare genetic mutation: at thirteen, his son weighs only 54 pounds, wears diapers, cannot speak and needs to wear special cuffs on his arms so that he cannot harm himself. Writ…
Title
The boy in the moon: A father's search for his disabled son
Author
Brown, Ian
Place
Toronto, ON
Publisher
Vintage Canada
Year Published
2010
Physical Description
Softcover; 295 p.
Topics
Parenting Children with Disabilities
Parenting Children with Physical Disabilities
Genetic Disorders
Abstract
This book tells the story of a father's personal journey and search for his disabled son. The author's son was born with a rare genetic mutation: at thirteen, his son weighs only 54 pounds, wears diapers, cannot speak and needs to wear special cuffs on his arms so that he cannot harm himself. Written with honesty and humour, this award winning book began as a Globe and Mail series.
ISBN
9780679310099
Language
English
Material Type
Book
Agency
BC Children's and Women's
Location
Family Support & Resource Centre
Audience
Patient or Public
Call Number
GK 655 BRO 2009
Copy 1 BC Children's and Women's Family Support & Resource Centre Available
thumbnail

Mind and body : Answers to your questions

https://libraries.phsa.ca/permalink/catalog113526

www.cdss.ca

Canadian Down Syndrome Society. Calgary, AB: Canadian Down Syndrome Society , 2014. — 2 copies, 2 available
Audience
Patient or Public
Agency
BC Children's and Women's
Location
Family Support & Resource Centre
Call Number
GI 310 CAN 2014
Mind and Body is a book written for self-advocates covering topics such as the male and female body, relationships, sexual safety, pregnancy, and abuse, plus much more. We wanted to make the most comprehensive sexuality resource there is for individuals with disabilities, so we collaborated with pr…
Title
Mind and body : Answers to your questions
Corporate Author
Canadian Down Syndrome Society
Place
Calgary, AB
Publisher
Canadian Down Syndrome Society
Year Published
2014
Physical Description
Letter from CDSS
Topics
Down Syndrome
Genetic Disorders
Abstract
Mind and Body is a book written for self-advocates covering topics such as the male and female body, relationships, sexual safety, pregnancy, and abuse, plus much more. We wanted to make the most comprehensive sexuality resource there is for individuals with disabilities, so we collaborated with professionals in the sexual education field.
Language
English
Agency
BC Children's and Women's
Location
Family Support & Resource Centre
URL
www.cdss.ca
Audience
Patient or Public
Call Number
GI 310 CAN 2014
Copy 1 BC Children's and Women's Family Support & Resource Centre Available
Copy 2 BC Children's and Women's Sunny Hill Education Resource Centre Missing

Encyclopedia of genetic disorders and birth defects

https://libraries.phsa.ca/permalink/catalog110555
Wynbrandt, James., Ludman, Mark D. New York, NY: Facts On File (Infobase) , 2008. 3rd ed. (Book) — 1 copy, 1 available
Audience
Professional
Agency
BC Children's and Women's
Location
Study & Learning Commons
Call Number
REF GI 20 WYN 2008
Topics cover everything from the most basic genetic concepts to the latest screening and diagnostic techniques. Coverage includes: ; autism, cancer, chromosomal abnormalities, ethics, genetic counseling, heart defects, muscular dystrophy, neural tube defects, phenylketonuria, spina bifida, and much…
Title
Encyclopedia of genetic disorders and birth defects
Author
Wynbrandt, James.
Ludman, Mark D.
Edition
3rd ed.
Place
New York, NY
Publisher
Facts On File (Infobase)
Year Published
2008
Physical Description
Hardcover, 682 p.
Topics
Genetics/Genetic Disorders-Encyclopedias
Genetic Disorders
Birth Defects. Congenital Abnormalities
Children's Health-Encyclopedias
UBC MD Undergrad
Abstract
Topics cover everything from the most basic genetic concepts to the latest screening and diagnostic techniques. Coverage includes:
autism, cancer, chromosomal abnormalities, ethics, genetic counseling, heart defects, muscular dystrophy, neural tube defects, phenylketonuria, spina bifida, and much more.
ISBN
9780816063963
Language
English
Material Type
Book
Agency
BC Children's and Women's
Location
Study & Learning Commons
Audience
Professional
Call Number
REF GI 20 WYN 2008
Copy 1 BC Children's and Women's Study & Learning Commons REF Available
thumbnail
Gorlin, Robert J., Cohen Jr., M. Michael, Hennekam, Raoul C. M. New York, N.Y.: Oxford University Press , 2001. Fourth edition. (Book) — 1 copy, 1 available
Audience
Professional
Agency
BC Children's and Women's
Location
Sunny Hill Education Resource Centre
Call Number
REF GI 20 GOR 2001
This illustrated text covers over 700 different genetic syndromes involving the head and neck inlcuding the phenotype spectrum, epidemiology, mode of inheritance and pathogenesis. Contents: Deformations and disruptions; Teratogenic agents; Chromosomal syndromes: Common and/or well-known syndromes;…
Title
Syndromes of the head and neck
Author
Gorlin, Robert J.
Cohen Jr., M. Michael
Hennekam, Raoul C. M.
Edition
Fourth edition
Place
New York, N.Y.
Publisher
Oxford University Press
Year Published
2001
Physical Description
Hard cover 1283 p.
Topics
Genetics/Genetic Disorders-Encyclopedias
Genetic Disorders
Birth Defects. Congenital Abnormalities
Children's Health. Pediatrics
Neck. Neck Disorders
Abstract
This illustrated text covers over 700 different genetic syndromes involving the head and neck inlcuding the phenotype spectrum, epidemiology, mode of inheritance and pathogenesis. Contents: Deformations and disruptions; Teratogenic agents; Chromosomal syndromes: Common and/or well-known syndromes; Chromosomal syndromes: Unusual variants; Metabolic disorders; Syndromes affecting bone: The osteogenesis imperfectas; Syndromes affecting bone: Chondrodysplasias and chondrodystrophies; Syndromes affecting bone: Craniotubular bone disorders; Syndromes affecting bone: Other skeletal dysplasias; Proportionate short stature syndromes; Overgrowth syndromes and postnatal onset obesity syndromes; Hamartoneoplastic syndromes; Syndromes affecting the skin and mucosa; Syndromes with craniosynostosis: General aspects and well-known syndromes; syndromes with craniosynostosis: miscellaneous syndromes; Syndromes of abnormal craniofacial contour; Syndromes affecting the central nervous system; Syndromes with contractures; Branchial arch and oro-acral disorders; Orofacial clefting syndromes: General aspects; Orofacial clefting syndromes: Common and well-known kyndromes; Orofacial clefting syndromes: Other syndromes; Orofacial clefting syndromes: Associations; Syndromes with unusual facies: Well-known syndromes; Syndromes with unusual facies: Other syndromes; Syndromes with gingival/periodontal components; Syndromes with unusual dental findings; Well-known miscellaneous syndromes; Other miscellaneous syndromes; Syndromes of the eye
ISBN
9780195118612
Language
English
Material Type
Book
Agency
BC Children's and Women's
Location
Sunny Hill Education Resource Centre
Audience
Professional
Call Number
REF GI 20 GOR 2001
Copy 1 BC Children's and Women's Sunny Hill Education Resource Centre REF / Redevelopment Available
thumbnail

Genetic and Rare Disease Information Center

https://libraries.phsa.ca/permalink/catalog104612

https://rarediseases.info.nih.gov/

National Human Genome Research Institute. Bethesda, MD: National Institutes of Health (Online)
Audience
Patient or Public
Agency
BC Children's and Women's
The Genetic and Rare Diseases Information Center employs experienced information specialists to answer questions from the general public, including patients and their families, health care professionals and biomedical researchers. Site includes comprehensive information sheets on 15 specific geneti…
Title
Genetic and Rare Disease Information Center
Corporate Author
National Human Genome Research Institute
Place
Bethesda, MD
Publisher
National Institutes of Health
Topics
Genetic Disorders
Genetics/Genetic Disorders-Directories. Resource Guides
Abstract
The Genetic and Rare Diseases Information Center employs experienced information specialists to answer questions from the general public, including patients and their families, health care professionals and biomedical researchers. Site includes comprehensive information sheets on 15 specific genetic disorders, including: Breast cancer
Charcot-Marie-Tooth; Colon cancer; Cystic fibrosis; Hemochromatosis; Huntington's disease; Parkinson's disease; Progeria; Sickle cell disease; Tay-Sachs; Thalassemia; Skin Cancer; Prostate Cancer.
Material Type
Online
Agency
BC Children's and Women's
URL
https://rarediseases.info.nih.gov/
Audience
Patient or Public

Genetics and mental retardation syndromes: A new look at behavior and interventions

https://libraries.phsa.ca/permalink/catalog104484
Dykens, Elisabeth M., Hodapp, Robert M., Finucane, Brenda M. Baltimore, MD: Paul H. Brookes Publishing Co. , 2000. (Book) — 1 copy, 1 available
Audience
Patient or Public
Agency
BC Children's and Women's
Location
Family Support & Resource Centre
Call Number
GI 300 DYK 2000
Identifies the genetic and behaviour characteristics of nine specific genetic syndromes. Four major syndromes (Down syndrome, Williams syndrome , Fragile-X syndrome, and Prader-Willi syndrome) are covered with in-depth information and five other syndromes are reveiwed (Velocardiofacial syndrome; R…
Title
Genetics and mental retardation syndromes: A new look at behavior and interventions
Author
Dykens, Elisabeth M.
Hodapp, Robert M.
Finucane, Brenda M.
Place
Baltimore, MD
Publisher
Paul H. Brookes Publishing Co.
Year Published
2000
Topics
Genetic Disorders
Down Syndrome
Fragile X Syndrome
Prader-Willi Syndrome
Abstract
Identifies the genetic and behaviour characteristics of nine specific genetic syndromes. Four major syndromes (Down syndrome, Williams syndrome , Fragile-X syndrome, and Prader-Willi syndrome) are covered with in-depth information and five other syndromes are reveiwed (Velocardiofacial syndrome; Rubinstein-Taybi syndrome; Smith-Magenis syndrome; Angelman syndrome and 5p- (cri-du-chat) syndrome).
ISBN
1-55766-471-4
Language
English
Material Type
Book
Agency
BC Children's and Women's
Location
Family Support & Resource Centre
Audience
Patient or Public
Call Number
GI 300 DYK 2000
Copy 1 BC Children's and Women's Family Support & Resource Centre Available
thumbnail

Care of the infant and child with Trisomy 18 or 13: Medical problems, reported treatments and milestones

https://libraries.phsa.ca/permalink/catalog104182
Barnes, Ann, Carey, John. Omaha, NE: Monroe-Meyer Institute for Genetics and Rehabilitation , 2000. Rev. ed. (Book) — 1 copy, 1 available
Audience
Patient or Public
Agency
BC Children's and Women's
Location
Family Support & Resource Centre
Call Number
GI 320 BAR 2000
Drawing from a combination of the literature and the support organization for Trisomy 18, 13 and Related Disorders (SOFT), this book deals with the daily living issues of children with trisomy. It includes feeding difficulties; postnatal growth; constipation; low muscle tone and neurological proble…
Title
Care of the infant and child with Trisomy 18 or 13: Medical problems, reported treatments and milestones
Author
Barnes, Ann
Carey, John
Edition
Rev. ed.
Place
Omaha, NE
Publisher
Monroe-Meyer Institute for Genetics and Rehabilitation
Year Published
2000
Physical Description
Softcover; 61 pp.
Topics
Edward Sydrome. Trisomy 18
Genetic Disorders
Abstract
Drawing from a combination of the literature and the support organization for Trisomy 18, 13 and Related Disorders (SOFT), this book deals with the daily living issues of children with trisomy. It includes feeding difficulties; postnatal growth; constipation; low muscle tone and neurological problems; common illnesses and problems; congenital anomalies; survival; morality and reported causes; milestones; and guidelines for recommended medical care. Contains many photographs.
Notes
Includes growth chart.
ISBN
1-889843-58-X
Language
English
Material Type
Book
Agency
BC Children's and Women's
Location
Family Support & Resource Centre
Audience
Patient or Public
Call Number
GI 320 BAR 2000
Copy 1 BC Children's and Women's Family Support & Resource Centre Available
thumbnail

Mendelian inheritance in man: A catalog of human genes and genetic disorders: Vol 1

https://libraries.phsa.ca/permalink/catalog112687

http://www.ncbi.nlm.nih.gov/omim

McKusiak, Victor A (Ed). Baltimore, MD: Johns Hopkins University Press , 1998. 12th Ed. (Book) — 2 copies, 2 available
Audience
Professional
Agency
BC Children's and Women's
Location
Study & Learning Commons
Call Number
REF GI 20 MCK 1998 VOL 1
URL Notes
The database corresponds to the print publication.
A comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.
Title
Mendelian inheritance in man: A catalog of human genes and genetic disorders: Vol 1
Author
McKusiak, Victor A (Ed).
Edition
12th Ed.
Place
Baltimore, MD
Publisher
Johns Hopkins University Press
Year Published
1998
Physical Description
Hardcover
Topics
Genetics
Genetic Disorders
Genetics/Genetic Disorders-Encyclopedias
Abstract
A comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.
ISBN
0801857422
Language
English
Material Type
Book
Agency
BC Children's and Women's
Location
Study & Learning Commons
URL
http://www.ncbi.nlm.nih.gov/omim
URL Notes
The database corresponds to the print publication.
Audience
Professional
Call Number
REF GI 20 MCK 1998 VOL 1
Copy 1 BC Children's and Women's Study & Learning Commons REF Available
Copy 2 BC Children's and Women's Study & Learning Commons REF Available
thumbnail

Mendelian inheritance in man: A catalog of human genes and genetic disorders: Vol 2

https://libraries.phsa.ca/permalink/catalog112688

http://www.ncbi.nlm.nih.gov/omim

McKusiak, Victor A (Ed). Baltimore, MD: Johns Hopkins University Press , 1998. 12th Ed. (Book) — 2 copies, 2 available
Audience
Professional
Agency
BC Children's and Women's
Location
Study & Learning Commons
Call Number
REF GI 20 MCK 1998 VOL 2
URL Notes
The database corresponds to the print publication.
A comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.
Title
Mendelian inheritance in man: A catalog of human genes and genetic disorders: Vol 2
Author
McKusiak, Victor A (Ed).
Edition
12th Ed.
Place
Baltimore, MD
Publisher
Johns Hopkins University Press
Year Published
1998
Physical Description
Hardcover
Topics
Genetics
Genetics/Genetic Disorders-Encyclopedias
Genetic Disorders
Abstract
A comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.
ISBN
0801857422
Language
English
Material Type
Book
Agency
BC Children's and Women's
Location
Study & Learning Commons
URL
http://www.ncbi.nlm.nih.gov/omim
URL Notes
The database corresponds to the print publication.
Audience
Professional
Call Number
REF GI 20 MCK 1998 VOL 2
Copy 1 BC Children's and Women's Study & Learning Commons REF Available
Copy 2 BC Children's and Women's Study & Learning Commons REF Available
thumbnail

Mendelian inheritance in man: A catalog of human genes and genetic disorders: Vol 3

https://libraries.phsa.ca/permalink/catalog112689

http://www.ncbi.nlm.nih.gov/omim

McKusiak, Victor A (Ed). Baltimore, MD: Johns Hopkins University Press , 1998. (Book) — 2 copies, 2 available
Audience
Professional
Agency
BC Children's and Women's
Location
Study & Learning Commons
Call Number
REF GI 20 MCK 1998 VOL 3
URL Notes
The database corresponds to the print publication.
A comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.
Title
Mendelian inheritance in man: A catalog of human genes and genetic disorders: Vol 3
Author
McKusiak, Victor A (Ed).
Place
Baltimore, MD
Publisher
Johns Hopkins University Press
Year Published
1998
Physical Description
Hardcover
Topics
Genetic Disorders
Genetics
Genetics/Genetic Disorders-Encyclopedias
Abstract
A comprehensive, authoritative and timely knowledgebase of human genes and genetic disorders compiled to support human genetics research and education and the practice of clinical genetics.
ISBN
0801857422
Language
English
Material Type
Book
Agency
BC Children's and Women's
Location
Study & Learning Commons
URL
http://www.ncbi.nlm.nih.gov/omim
URL Notes
The database corresponds to the print publication.
Audience
Professional
Call Number
REF GI 20 MCK 1998 VOL 3
Copy 1 BC Children's and Women's Study & Learning Commons REF Available
Copy 2 BC Children's and Women's Study & Learning Commons REF Available
thumbnail

[First ever] national conference on Trisomy X and XYY: The genetics

https://libraries.phsa.ca/permalink/catalog110355
M.I.N.D. Institute. Coto de Caza, CA: KS&A , 2006. (Video) — 1 copy, 1 available
Audience
Patient or Public
Agency
BC Children's and Women's
Location
Family Support & Resource Centre
Call Number
GI 300 FIR 2006
Excerpts from two full days of meetings (March 3-5, 2006) focusing on the needs and issues of Trisomy X and XYY. Features Dr. Patricia Jacobs and Dr. Terry Hassold.
Title
[First ever] national conference on Trisomy X and XYY: The genetics
Corporate Author
M.I.N.D. Institute
Place
Coto de Caza, CA
Publisher
KS&A
Year Published
2006
Physical Description
1 DVD
Topics
Genetic Disorders
XYY Male
Genetics
Abstract
Excerpts from two full days of meetings (March 3-5, 2006) focusing on the needs and issues of Trisomy X and XYY. Features Dr. Patricia Jacobs and Dr. Terry Hassold.
Language
English
Material Type
Video
Agency
BC Children's and Women's
Location
Family Support & Resource Centre
Audience
Patient or Public
Call Number
GI 300 FIR 2006
Copy 1 BC Children's and Women's Family Support & Resource Centre Available

17 records – page 1 of 1.