Mutation at the anophthalmic white locus in Syrian hamsters: haploinsufficiency in the Mitf gene mimics human Waardenburg syndrome type 2

By Hodgkinson C.A.  

Human Molecular Genetics, Vol. 7, Iss. 4, 1998-04 ,pp. : 703-708

Oxford University Press

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A dinucleotide mutation in the endothelin-B receptor gene is associated with lethal white foal syndrome (LWFS); a horse variant of Hirschsprung disease (HSCR)

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Human Molecular Genetics, Vol. 7, Iss. 6, 1998-06 ,pp. : 1047-1053

Oxford University Press

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Molecular characterization of the Arginine decarboxylase gene family in rice

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Transgenic Research, Vol. 19, Iss. 5, 2010-10 ,pp. : 785-797

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The white-phase-specific gene WH11 is not required for white-opaque switching in Candida albicans

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Characterization of a Nonsense Mutation in the Ceruloplasmin Gene Resulting in Diabetes and Neurodegenerative Disease

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