Case–control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8

By Chen Wu-Yan  

Human Molecular Genetics, Vol. 13, Iss. 23, 2004-12 ,pp. : 2991-2995

Oxford University Press

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Characterization of a Second Human Clathrin Heavy Chain Polypeptide Gene ( CLH-22 ) from Chromosome 22q11

By Kedra Darek   Peyrard Myriam   Fransson Ingegerd   Collins John E.   Dunham Ian   Roe Bruce A.   Dumanski Jan P.  

Human Molecular Genetics, Vol. 5, Iss. 5, 1996-01 ,pp. : 625-631

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Spontaneous deletion of epilepsy gene orthologs in a mutant mouse with a low electroconvulsive threshold

By Yang Y.  

Human Molecular Genetics, Vol. 12, Iss. 9, 2003-05 ,pp. : 975-984

Oxford University Press

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The 22q11 deletion syndromes

By Scambler Peter J.  

Human Molecular Genetics, Vol. 9, Iss. 16, 2000-10 ,pp. : 2421-2426

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Dissection of Tbx1 and Fgf interactions in mouse models of 22q11DS suggests functional redundancy

By Aggarwal Vimla S.   Liao Jun   Schimmang Thomas   Lewandoski Mark   Locker Joseph   Shanske Alan   Campione Marina   Morrow Bernice E.  

Human Molecular Genetics, Vol. 15, Iss. 21, 2006-11 ,pp. : 3219-3228

Oxford University Press

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