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Statements

Subject Item

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tieteellinen artikkeli vedecký článok scientific article published in September 1997 מאמר מדעי artikel ilmiah 1997年學術文章 artigo científico scienca artikolo 1997年学术文章 article scientifique article scientific мақолаи илмӣ სამეცნიერო სტატია scientific article published in September 1997 1997年學術文章 vědecký článek 1997年学术文章 articolo scientifico teaduslik artikkel 1997 nî lūn-bûn artikull shkencor tudományos cikk مقالة علمية نشرت في سبتمبر 1997 บทความทางวิทยาศาสตร์ vitskapeleg artikkel artykuł naukowy naučni članak 1997年學術文章 artigo científico vetenskaplig artikel научна статия 1997年学术文章 научни чланак wetenschappelijk artikel наукова стаття, опублікована у вересні 1997 1997年學術文章 সেপ্টেম্বর ১৯৯৭-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ vitenskapelig artikkel artículo científico publicado en 1997 scientific article published in September 1997 artikulong pang-agham научни чланак articol științific wissenschaftlicher Artikel 1997年学术文章 επιστημονικό άρθρο 1997年學術文章 1997年の論文 1997年学术文章 bilimsel makale artigo científico научная статья bài báo khoa học 1997年学术文章 artículu científicu 1997년 논문 videnskabelig artikel article científic

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1997-09-01T00:00:00Z

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L Zelante K Delgrosso N Govea E Rappaport M Shohat M Milá L D'Agruma P Fortina J Lutfi E Mansfield M D Monica S Surrey S Melchionda P Gasparini

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Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness

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Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans.

schema:name

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness

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Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans.

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1605-1609

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n11:9285800

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9285800

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9

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wds:Q48045551-D3E22712-0766-4016-B415-DD53795EE8CA

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n12:6.9.1605

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10.1093/HMG/6.9.1605

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wds:Q48045551-9C6EEDFF-7FC5-4091-888C-4279258598EB

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277549233