The Murine Homologue of HIRA, a DiGeorge Syndrome Candidate Gene, Is Expressed in Embryonic Structures Affected in Human CATCH22 Patients

By Wilming Laurens G.   Snoeren C. A. Sylvia   van Rijswijk Angelique   Grosveld Frank   Meijers Carel  

Human Molecular Genetics, Vol. 6, Iss. 2, 1997-01 ,pp. : 247-258

Oxford University Press

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ES2 , a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene

By Harvey E.L.  

Human Molecular Genetics, Vol. 7, Iss. 4, 1998-04 ,pp. : 629-635

Oxford University Press

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The Necdin Gene is Deleted in Prader-Willi Syndrome and is Imprinted in Human and Mouse

By MacDonald Heather R.   Wevrick Rachel  

Human Molecular Genetics, Vol. 6, Iss. 11, 1997-10 ,pp. : 1873-1878

Oxford University Press

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The 22q11 deletion syndrome candidate gene Tbx1 determines thyroid size and positioning

By Fagman H.   Liao J.   Westerlund J.   Andersson L.   Morrow B.E.   Nilsson M.  

Human Molecular Genetics, Vol. 16, Iss. 3, 2007-02 ,pp. : 276-285

Oxford University Press

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WBSCR14 , a gene mapping to the Williams–Beuren syndrome deleted region, is a new member of the Mlx transcription factor network

By Cairo S.   Merla G.   Urbinati F.   Ballabio A.   Reymond A.  

Human Molecular Genetics, Vol. 10, Iss. 6, 2001-03 ,pp. : 617-627

Oxford University Press

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