Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness

By Balkany T.  

Human Molecular Genetics, Vol. 10, Iss. 25, 2001-12 ,pp. : 2945-2951

Oxford University Press

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Connexin26 Mutations Associated with the Most Common Form of Non-Syndromic Neurosensory Autosomal Recessive Deafness (DFNB1) in Mediterraneans

By Zelante Leopoldo   Gasparini Paolo   Estivill Xavier  

Human Molecular Genetics, Vol. 6, Iss. 9, 1997-01 ,pp. : 1605-1609

Oxford University Press

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Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1

By Griffin A.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2509-2514

Oxford University Press

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CHX10 mutations cause non-syndromic microphthalmia/anophthalmia in Arab and Jewish kindreds

By Bar-Yosef Udy   Abuelaish Izzeldin   Harel Tamar   Hendler Neta   Ofir Rivka   Birk Ohad  

Human Genetics, Vol. 115, Iss. 4, 2004-09 ,pp. : 302-309

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Identification of two AGTR2 mutations in male patients with non-syndromic mental retardation

By Ylisaukko-oja Tero   Rehnström Karola   Vanhala Raija   Tengström Carola   Lähdetie Jaana   Järvelä Irma  

Human Genetics, Vol. 114, Iss. 2, 2004-01 ,pp. : 211-213

Springer Publishing Company

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