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A second Middle Eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9
A second kindred has been identified which supports the previously reported location of DFNB9. Linkage has been established to markers closely linked to DFNB9 which is located on 2p22-p23. The hearing impaired individuals in this highly consanguineous kindred from Eastern Turkey have prelingual prof...
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| Yayımlandı: | Eur J Hum Genet |
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| Asıl Yazarlar: | , , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
1998
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6141006/ https://ncbi.nlm.nih.gov/pubmed/9781041 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.ejhg.5200201 |
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