Nonhomologous Recombination between the Cytochrome b 558 Heavy Chain Gene (CYBB) and LINE-1 Causes an X-Linked Chronic Granulomatous Disease

By Kumatori A.   Faizunnessa N.N.   Suzuki S.   Moriuchi T.   Kurozumi H.   Nakamura M.  

Genomics, Vol. 53, Iss. 2, 1998-10 ,pp. : 123-128

Elsevier

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Cloning and Characterization of CLCN5, the Human Kidney Chloride Channel Gene Implicated in Dent Disease (an X-Linked Hereditary Nephrolithiasis)

By F Isher S.I.E.   van B Akel I.N.   L Loyd S.A.E.   P Earce S.I.H.S.   T Hakker R.A.V.   C Raig I.A.W.  

Genomics, Vol. 29, Iss. 3, 1995-10 ,pp. : 598-606

Academic Press

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Characterization of Novel Promoter and Enhancer Elements of the Mouse Homologue of the Dent Disease Gene, CLCN5, Implicated in X-Linked Hereditary Nephrolithiasis

By Tanaka K.   Fisher S.E.   Craig I.W.  

Genomics, Vol. 58, Iss. 3, 1999-06 ,pp. : 281-292

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Mapping and Characterization of the X-Linked Dyskeratosis Congenita (DKC) Gene

By Hassock S.   Vetrie D.   Giannelli F.  

Genomics, Vol. 55, Iss. 1, 1999-01 ,pp. : 21-27

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Partial Deletion of both the Spermine Synthase Gene and thePexGene in the X-linked Hypophosphatemic, Gyro (Gy) Mouse

By Meyer R.A.   Henley C.M.   Meyer M.H.   Morgan P.L.   McDonald A.G.   Mills C.   Price D.K.  

Genomics, Vol. 48, Iss. 3, 1998-03 ,pp. : 289-295

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