The Location of HumanCASKat Xp11.4 Identifies This Gene as a Candidate for X-Linked Optic Atrophy

By Dimitratos S.D.   Stathakis D.G.   Nelson C.A.   Woods D.F.   Bryant P.J.  

Genomics, Vol. 51, Iss. 2, 1998-07 ,pp. : 308-309

Elsevier

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Novel NPR1 polymorphic variants and its exclusion as a candidate gene for medullary cystic kidney disease (ADMCKD) type 1

By Koptides M.   Mean R.   Stavrou C.   Pierides A.   Demetriou K.   Nakayama T.   Hildebrandt F.   Fuchshuber A.   Deltas C.C.  

Molecular and Cellular Probes, Vol. 15, Iss. 6, 2001-12 ,pp. : 357-361

Elsevier

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Increased Gene Dosage at Xq26–q27 Is Associated with X-Linked Hypopituitarism

By Solomon N.M.   Nouri S.   Warne G.L.   Lagerström-Fermér M.   Forrest S.M.   Thomas P.Q.  

Genomics, Vol. 79, Iss. 4, 2002-04 ,pp. : 553-559

Academic Press

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Characterization of the Human Glutamate Receptor Subunit 3 Gene (GRIA3), a Candidate for Bipolar Disorder and Nonspecific X-Linked Mental Retardation

By Gecz J.   Barnett S.   Liu J.   Hollway G.   Donnelly A.   Eyre H.   Eshkevari H.S.   Baltazar R.   Grunn A.   Nagaraja R.   Gilliam C.   Peltonen L.   Sutherland G.R.   Baron M.   Mulley J.C.  

Genomics, Vol. 62, Iss. 3, 1999-12 ,pp. : 356-368

Elsevier

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cDNA Cloning of the Murine Pex Gene Implicated in X-Linked Hypophosphatemia and Evidence for Expression in Bone

By Du L.   desbarats M.   Viel J.   Glorieux F.H.   Cawthorn C.   Ecarot B.  

Genomics, Vol. 36, Iss. 1, 1996-08 ,pp. : 22-28

Academic Press

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