Gene expression analysis in a canine model of X-linked Alport syndrome

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Mammalian Genome, Vol. 17, Iss. 9, 2006-09 ,pp. : 976-990

Springer Publishing Company

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Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis

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Human Molecular Genetics, Vol. 14, Iss. 13, 2005-07 ,pp. : 1795-1803

Oxford University Press

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Mutations in the RPGR gene cause X-linked cone dystrophy

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Human Molecular Genetics, Vol. 11, Iss. 5, 2002-03 ,pp. : 605-611

Oxford University Press

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Identification of a Gene Disrupted by a Microdeletion in a Patient with X-Linked Retinitis Pigmentosa (XLRP)

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Distribution of Mutations in the PEX Gene in Families with X-linked Hypophosphataemic Rickets (HYP)

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