Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population-Reference-Cited by-同舟云学术

Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population

Published:2006-01-01 Issue:4 Volume:2 Page:
ISSN:1479-7364
Container-title:Human Genomics
language:en
Short-container-title:Hum Genomics

Author:

Walsh Tom,Rayan Amal Abu,Sa'ed Judeh Abu,Shahin Hashem,Shepshelovich Jeanne,Lee Ming K,Hirschberg Koret,Tekin Mustafa,Salhab Wa'el,Avraham Karen B,King Mary-Claire,Kanaan Moien

Publisher

Springer Science and Business Media LLC

Subject

Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1186/1479-7364-2-4-203.pdf

Reference37 articles.

1. Jaber L, Halpern GJ, Shohat T: Trends in the frequencies of consanguineous marriages in the Israeli Arab community. Clin Genet. 2000, 58: 106-110.

2. Zlotogora J: Molecular basis of autosomal recessive diseases among the Palestinian Arabs. Am J Med Genet. 109: 176-182.

3. Kent WJ, Sugnet CW, Furey TS, et al: The Human Genome Browser at UCSC. Genome Res. 2002, 12: 996-1006.

4. Walsh T, Walsh V, Vreugde S, et al: From flies' eyes to our ears: Mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30. Proc Natl Acad Sci USA. 2002, 99: 7518-7523. 10.1073/pnas.102091699.

5. Scott HS, Kudoh J, Wattenhofer M, et al: Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness. Nat Genet. 2001, 27: 59-63.

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