Publication
| Schultz JM, Khan SN, Ahmed ZM, Riazuddin S, Waryah AM, Chhatre D, Starost MF, Ploplis B, Buckley S, Velásquez D, Kabra M, Lee K, Hassan MJ, Ali G, Ansar M, Ghosh M, Wilcox ER, Ahmad W, Merlino G, Leal SM, Riazuddin S, Friedman TB, Morell RJ, Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39 American journal of human genetics85:25-39 2009 |
| PubMed ID: 19576567 |
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| Records Return:
(6)
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| Catalog ID | Gender | Age at Sampling | Family | Relationship | Description | Collection_Type_id |
| GM20199 | Male | 65 YR | 2462 | father | DEAFNESS, AUTOSOMAL RECESSIVE 39; DFNB39 | GM |
| GM20198 | Male | 18 YR | 2462 | proband | DEAFNESS, AUTOSOMAL RECESSIVE 39; DFNB39 | GM |
| GM20174 | Male | 58 YR | 2450 | father | DEAFNESS, AUTOSOMAL RECESSIVE 39; DFNB39 | GM |
| GM20175 | Male | 20 YR | 2450 | proband | DEAFNESS, AUTOSOMAL RECESSIVE 39; DFNB39 | GM |
| GM20170 | Female | 40 YR | 2448 | mother | DEAFNESS, AUTOSOMAL RECESSIVE 39; DFNB39 | GM |
| GM20171 | Female | 17 YR | 2448 | proband | DEAFNESS, AUTOSOMAL RECESSIVE 39; DFNB39 | GM |
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