Domain disruption and mutation of the bZIP transcription factor, MAF , associated with cataract, ocular anterior segment dysgenesis and coloboma

By Munier F.  

Human Molecular Genetics, Vol. 11, Iss. 1, 2002-01 ,pp. : 33-42

Oxford University Press

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Mutations of a human homologue of the Drosophila eyes absent gene ( EYA1 ) detected in patients with congenital cataracts and ocular anterior segment anomalies

By Azuma Noriyuki  

Human Molecular Genetics, Vol. 9, Iss. 3, 2000-02 ,pp. : 363-366

Oxford University Press

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Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy

By Van Agtmael Tom  

Human Molecular Genetics, Vol. 14, Iss. 21, 2005-11 ,pp. : 3161-3168

Oxford University Press

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Anterior segment dysgenesis and the developmental glaucomas are complex traits

By Gould D.B.   John S.W.M.  

Human Molecular Genetics, Vol. 11, Iss. 10, 2002-05 ,pp. : 1185-1193

Oxford University Press

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Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld–Rieger syndrome and anterior segment dysgenesis

By Berry Fred B.   Lines Matthew A.   Footz Tim   Underhill D. Alan   Gage Philip J.   Walter Michael A.  

Human Molecular Genetics, Vol. 15, Iss. 6, 2006-03 ,pp. : 905-919

Oxford University Press

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