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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Isolation and Characterization of a Human Gene Containing a Nuclear Localization Signal from the Critical Region for Velo-Cardio-Facial Syndrome on 22q11

By Funke B.   Puech A.   Saint-Jore B.   Pandita R.   Skoultchi A.   Morrow B.  

Genomics, Vol. 53, Iss. 2, 1998-10 ,pp. : 146-154

Elsevier

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Isolation and Characterization of a Novel Gene Containing WD40 Repeats from the Region Deleted in Velo-cardio-facial/ DiGeorge Syndrome on Chromosome 22q11

By Funke B.   Pandita R.K.   Morrow B.E.  

Genomics, Vol. 73, Iss. 3, 2001-05 ,pp. : 264-271

Elsevier

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MLL3, a new human member of the TRX/MLL gene family, maps to 7q36, a chromosome region frequently deleted in myeloid leukaemia

By Ruault M.   Brun M.E.   Ventura M.   Roizes G.   De Sario A.  

Gene, Vol. 284, Iss. 1, 2002-02 ,pp. : 73-81

Elsevier

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A New Gene Family Including DSCR1 (Down Syndrome Candidate Region 1) and ZAKI-4: Characterization from Yeast to Human and Identification of DSCR1-like 2, a Novel Human Member (DSCR1L2)

By Strippoli P.   Lenzi L.   Petrini M.   Carinci P.   Zannotti M.  

Genomics, Vol. 64, Iss. 3, 2000-03 ,pp. : 252-263

Elsevier

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