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| Year | Number of Results |
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| 2003 | 2 |
| 2004 | 1 |
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A homozygous GJA1 gene mutation causes a Hallermann-Streiff/ODDD spectrum phenotype.
Hum Mutat. 2004 Mar;23(3):286. doi: 10.1002/humu.9220.
Hum Mutat. 2004.
PMID: 14974090
A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1-14q24.3 in large consanguineous kindred from Pakistan.
Ansar M, Din MA, Arshad M, Sohail M, Faiyaz-Ul-Haque M, Haque S, Ahmad W, Leal SM.
Ansar M, et al.
Eur J Hum Genet. 2003 Jan;11(1):77-80. doi: 10.1038/sj.ejhg.5200905.
Eur J Hum Genet. 2003.
PMID: 12529709
Free PMC article.
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Localization of a novel autosomal recessive non-syndromic hearing impairment locus (DFNB38) to 6q26-q27 in a consanguineous kindred from Pakistan.
Ansar M, Ramzan M, Pham TL, Yan K, Jamal SM, Haque S, Ahmad W, Leal SM.
Ansar M, et al.
Hum Hered. 2003;55(1):71-4. doi: 10.1159/000071813.
Hum Hered. 2003.
PMID: 12890929
Free PMC article.
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