Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA

By Litt M.  

Human Molecular Genetics, Vol. 7, Iss. 3, 1998-03 ,pp. : 471-474

Oxford University Press

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γ 2-COP , a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome

By Blagitko Nadya  

Human Molecular Genetics, Vol. 8, Iss. 13, 1999-12 ,pp. : 2387-2396

Oxford University Press

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Autosomal Dominant Cerulean Cataract Is Associated with a Chain Termination Mutation in the Human β-Crystallin Gene CRYBB2

By Litt Michael  

Human Molecular Genetics, Vol. 6, Iss. 5, 1997-01 ,pp. : 665-668

Oxford University Press

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A large polymorphic repeat in the pericentromeric region of human chromosome 15q contains three partial gene duplications

By Ritchie R.J.   Mattei M-G.   Lalande M.  

Human Molecular Genetics, Vol. 7, Iss. 8, 1998-08 ,pp. : 1253-1260

Oxford University Press

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A 5-base insertion in the γC-crystallin gene is associated with autosomal dominant variable zonular pulverulent cataract

By Ren Zhaoxia   Li Anren   Shastry Barker S.   Padma Tirunilai   Ayyagari Radha   Scott Mark H.   Parks Marshall M.   Kaiser-Kupfer Muriel I.   Hejtmancik J. Fielding  

Human Genetics, Vol. 106, Iss. 5, 2000-05 ,pp. : 531-537

Springer Publishing Company

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