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

By Roepman Ronald   Bauer David   Rosenberg Thomas   van Duijnhoven Gerard   van de Vosse Esther   Platzer Matthias   Rosenthal André   Ropers Hans-Hilger   Cremers Frans P. M.   Berger Wolfgang  

Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 827-833

Oxford University Press

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Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28

By Gigarel Nadine   Frydman Nelly   Burlet Philippe   Kerbrat Violaine   Steffann Julie   Frydman René   Munnich Arnold   Ray Pierre  

Human Genetics, Vol. 114, Iss. 3, 2004-02 ,pp. : 298-305

Springer Publishing Company

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Decreased expression of ABCD4 and BG1 genes early in the pathogenesis of X-linked adrenoleukodystrophy

By Asheuer Muriel  

Human Molecular Genetics, Vol. 14, Iss. 10, 2005-05 ,pp. : 1293-1303

Oxford University Press

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Mid1/Mid2 expression in craniofacial development and a literature review of X‐linked opitz syndrome

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Molecular Genetics & Genomic Medicine, Vol. 4, Iss. 1, 2016-01 ,pp. : 95-105

John Wiley & Sons Inc

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A Model of Corrective Gene Transfer in X-Linked Ichthyosis

By Freiberg Rachel A.  

Human Molecular Genetics, Vol. 6, Iss. 6, 1997-01 ,pp. : 927-933

Oxford University Press

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