Genetic Heterogeneity of Usher Syndrome: Analysis of 151 Families with Usher Type I-Reference-Cited by-同舟云学术

Genetic Heterogeneity of Usher Syndrome: Analysis of 151 Families with Usher Type I

Published:2000-12 Issue:6 Volume:67 Page:1569-1574
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Astuto Lisa M.,Weston Michael D.,Carney Carol A.,Hoover Denise M.,Cremers Cor W.R.J.,Wagenaar Mariette,Moller Claes,Smith Richard J.H.,Pieke-Dahl Sandra,Greenberg Jacquie,Ramesar Raj,Jacobson Samuel G.,Ayuso Carmen,Heckenlively John R.,Tamayo Marta,Gorin Michael B.,Reardon Willie,Kimberling William J.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference27 articles.

1. A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene;Bitner-Glindzicz;J Med Genet,2000

2. Usher syndrome: definition and estimate of prevalence from two high-risk populations;Boughman;J Chronic Dis,1983

3. A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21;Chaib;Hum Mol Genet,1997

4. Linkage analysis in USH1 families from Spain;Espinos;J Med Genet,1998

5. Usher syndrome type III (USH3) linked to chromosome 3q in an Italian family;Gasparini;J Med Genet,1998

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