The Genomic Structure of the Gene Defective in Usher Syndrome Type Ib (MYO7A)

By Kelley P.M.   Weston M.D.   Chen Z.Y.   Orten D.J.   Hasson T.   Overbeck L.D.   Pinnt J.   Talmadge C.B.   Ing P.   Mooseker M.S.   Corey D.   Sumegi J.   Kimberling W.J.  

Genomics, Vol. 40, Iss. 1, 1997-02 ,pp. : 73-79

Academic Press

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Molecular Cloning and Domain Structure of Human Myosin-VIIa, the Gene Product Defective in Usher Syndrome 1B

By Chen Z.Y.   Hasson T.   Kelley P.M.   Schwender B.J.   Schwartz M.F.   Ramakrishnan M.   Kimberling W.J.   Mooseker M.S.   Corey D.P.  

Genomics, Vol. 36, Iss. 3, 1996-09 ,pp. : 440-448

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A novel mutation in the MITF gene causes Waardenburg Syndrome Type 2

By Lautenschlager N.T.   Milunsky A.   DeStefano A.   Farrer L.   Baldwin C.T.  

Genetic Analysis: Biomolecular Engineering, Vol. 13, Iss. 2, 1996-07 ,pp. : 43-44

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Isolation of a Gene Encoding a Novel Member of the Nuclear Receptor Superfamily from the Critical Region of Usher Syndrome Type IIa at 1q41

By Eudy J.D.   Yao S.   Weston M.D.   Ma-Edmonds M.   Talmadge C.B.   Cheng J.J.   Kimberling W.J.   Sumegi J.  

Genomics, Vol. 50, Iss. 3, 1998-06 ,pp. : 382-384

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Isolation of a Novel Human Homologue of the Gene Coding for Echinoderm Microtubule-Associated Protein (EMAP) from the Usher Syndrome Type 1a Locus at 14q32

By Eudy J.D.   Ma-Edmonds M.   Yao S.   Talmadge C.B.   Kelley P.M.   Weston M.D.   Kimberling W.J.   Sumegi J.  

Genomics, Vol. 43, Iss. 1, 1997-07 ,pp. : 104-106

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