DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3-Reference-Cited by-同舟云学术

DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3

Published:2009-07-15 Issue:1 Volume:18 Page:125-129
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Khan Shahid Yar,Riazuddin Saima,Shahzad Mohsin,Ahmed Nazir,Zafar Ahmad Usman,Rehman Atteeq Ur,Morell Robert J,Griffith Andrew J,Ahmed Zubair M,Riazuddin Sheikh,Friedman Thomas B

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg2009121.pdf

Reference16 articles.

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2. Morton CC, Nance WE : Newborn hearing screening—a silent revolution. N Engl J Med 2006; 354: 2151–2164.

3. Medlej-Hashim M, Mustapha M, Chouery E et al: Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations. Eur J Hum Genet 2002; 10: 391–394.

4. Belguith H, Masmoudi S, Medlej-Hashim M et al: Re-assigning the DFNB33 locus to chromosome 10p11.23-q21.1. Eur J Hum Genet 2009; 17: 122–124.

5. Grimberg J, Nawoschik S, Belluscio L, McKee R, Turck A, Eisenberg A : A simple and efficient non-organic procedure for the isolation of genomic DNA from blood. Nucleic Acids Res 1989; 17: 8390.

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