Identification of SCML2, a Second Human Gene Homologous to theDrosophila Sex comb on midleg(Scm): A New Gene Cluster on Xp22

By Montini E.   Buchner G.   Spalluto C.   Andolfi G.   Caruso A.   den Dunnen J.T.   Trump D.   Rocchi M.   Ballabio A.   Franco B.  

Genomics, Vol. 58, Iss. 1, 1999-05 ,pp. : 65-72

Elsevier

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Characterization ofSCML1,a New Gene in Xp22, with Homology to Developmental Polycomb Genes

By van de Vosse E.   Walpole S.M.   Nicolaou A.   van der Bent P.   Cahn A.   Vaudin M.   Ross M.T.   Durham J.   Pavitt R.   Wilkinson J.   Grafham D.   Bergen A.A.B.   van Ommen G.-J.B.   Yates J.R.W.   den Dunnen J.T.   Trump D.  

Genomics, Vol. 49, Iss. 1, 1998-04 ,pp. : 96-102

Elsevier

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Identification and Characterization of the Human Homologue (RAI2) of a Mouse Retinoic Acid-Induced Gene in Xp22

By Walpole S.M.   Hiriyana K.T.   Nicolaou A.   Bingham E.L.   Durham J.   Vaudin M.   Ross M.T.   Yates J.R.W.   Sieving P.A.   Trump D.  

Genomics, Vol. 55, Iss. 3, 1999-02 ,pp. : 275-283

Elsevier

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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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The Human Inward Rectifying K+ Channel Kir 2.2 (KCNJ12) Gene: Gene Structure, Assignment to Chromosome 17p11.1, and Identification of a Simple Tandem Repeat Polymorphism

By Hugnot J.P.   Pedeutour F.   Le Calvez C.   Grosgeorge J.   Passage E.   Fontes M.   Lazdunski M.  

Genomics, Vol. 39, Iss. 1, 1997-01 ,pp. : 113-116

Academic Press

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