Novel Mutations of the Endothelin-B Receptor Gene in Isolated Patients with Hirschsprung'S Disease

By Kusafuka Takeshi   Wang Yiping   Puri Prem  

Human Molecular Genetics, Vol. 5, Iss. 3, 1996-01 ,pp. : 347-349

Oxford University Press

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Endothelin-B Receptor Mutations in Patients with Isolated Hirschsprung Disease from a Non-Inbred Population

By Auricchio Alberto   Casari Giorgio   Staiano Annamaria   Ballabio Andrea  

Human Molecular Genetics, Vol. 5, Iss. 3, 1996-01 ,pp. : 351-354

Oxford University Press

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A dinucleotide mutation in the endothelin-B receptor gene is associated with lethal white foal syndrome (LWFS); a horse variant of Hirschsprung disease (HSCR)

By Yang G.C.   Croaker D.   Zhang A.L.   Manglick P.   Cartmill T.   Cass D.  

Human Molecular Genetics, Vol. 7, Iss. 6, 1998-06 ,pp. : 1047-1053

Oxford University Press

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The endothelin receptor B ( EDNRB ) promoter displays heterogeneous, site specific methylation patterns in normal and tumor cells

By Pao M.M.  

Human Molecular Genetics, Vol. 10, Iss. 9, 2001-04 ,pp. : 903-910

Oxford University Press

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Interactions between Sox10 and EdnrB modulate penetrance and severity of aganglionosis in the Sox10Dom mouse model of Hirschsprung disease

By Cantrell V. Ashley   Owens Sarah E.   Chandler Ronald L.   Airey David C.   Bradley Kevin M.   Smith Jeffrey R.   Southard-Smith E. Michelle  

Human Molecular Genetics, Vol. 13, Iss. 24, 2004-12 ,pp. : 3241-3241

Oxford University Press

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