Clinical genetics and the Hutterite population: A review of Mendelian disorders-Reference-Cited by-同舟云学术

Clinical genetics and the Hutterite population: A review of Mendelian disorders

Published:2008 Issue:8 Volume:146A Page:1088-1098
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Boycott Kym M.,Parboosingh Jillian S.,Chodirker Bernie N.,Lowry R. Brian,McLeod D. Ross,Morris Jackie,Greenberg Cheryl R.,Chudley Albert E.,Bernier Francois P.,Midgley Julian,Møller Lisbeth Birk,Innes A. Micheil

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference84 articles.

1. Dihydropyrimidine Dehydrogenase Deficiency in a Hutterite Newborn

2. Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

3. Genetics of population isolates

4. Leu-676-Pro mutation of the androgen receptor causes complete androgen insensitivity syndrome in a large Hutterite kindred

5. Workshop on genetic disorders in the Hutterites—Edmonton, Canada, October 12-13, 1983

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