LETM1, a gene deleted in Wolf-Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein

By Schlickum S.   Moghekar A.   Simpson J.C.   Steglich C.   O'Brien R.J.   Winterpacht A.   Endele S.U.  

Genomics, Vol. 83, Iss. 2, 2004-02 ,pp. : 254-261

Elsevier

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Comparative Analysis of a Novel Gene from the Wolf-Hirschhorn/Pitt-Rogers-Danks Syndrome Critical Region

By Wright T.J.   Costa J.L.   Naranjo C.   Francis-West P.   Altherr M.R.  

Genomics, Vol. 59, Iss. 2, 1999-07 ,pp. : 203-212

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RAI1 is a novel polyglutamine encoding gene that is deleted in Smith-Magenis syndrome patients

By Seranski P.   Hoff C.   Radelof U.   Hennig S.   Reinhardt R.   Schwartz C.E.   Heiss N.S.   Poustka A.  

Gene, Vol. 270, Iss. 1, 2001-05 ,pp. : 69-76

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Identification, Characterization, and Precise Mapping of a Human Gene Encoding a Novel Membrane-Spanning Protein from the 22q11 Region Deleted in Velo-Cardio-Facial Syndrome

By Sirotkin H.   Morrow B.   Saint-Jore B.   Puech A.   Gupta R.D.   Patanjali S.R.   Skoultchi A.   Weissman S.M.   Kucherlapati R.  

Genomics, Vol. 42, Iss. 2, 1997-06 ,pp. : 245-251

Academic Press

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Cloning and characterization of a novel gene, SHPRH, encoding a conserved putative protein with SNF2/helicase and PHD-finger domains from the 6q24 region*

By Sood R.   Makalowska I.   Galdzicki M.   Hu P.   Eddings E.   Robbins C.M.   Moses T.   Namkoong J.   Chen S.   Trent J.M.  

Genomics, Vol. 82, Iss. 2, 2003-08 ,pp. : 153-161

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