A molecular analysis of the Yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies

By Bondurand Nadège   Kuhlbrodt Kirsten  

Human Molecular Genetics, Vol. 8, Iss. 9, 1999-09 ,pp. : 1785-1789

Oxford University Press

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Duplication of SOX3 (Xq27) may be a risk factor for Neural Tube Defects

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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 7, 2015-07 ,pp. : 1676-1678

John Wiley & Sons Inc

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Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1

By Wat Margaret J.   Beck Tyler F.   Hernández-García Andrés   Yu Zhiyin   Veenma Danielle   Garcia Monica   Holder Ashley M.   Wat Jeanette J.   Chen Yuqing   Mohila Carrie A.   Lally Kevin P.   Dickinson Mary   Tibboel Dick   de Klein Annelies   Lee Brendan   Scott Daryl A.  

Human Molecular Genetics, Vol. 21, Iss. 18, 2012-09 ,pp. : 4115-4125

Oxford University Press

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Genetic background impacts developmental potential of enteric neural crest-derived progenitors in the Sox10 Dom model of Hirschsprung disease

By Walters Lauren C.   Cantrell V. Ashley   Weller Kevin P.   Mosher Jack T.   Southard-Smith E. Michelle  

Human Molecular Genetics, Vol. 19, Iss. 22, 2010-11 ,pp. : 4353-4372

Oxford University Press

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Structure–function analysis reveals the molecular determinants of the impaired biological function of DAX-1 mutants in AHC patients

By Lehmann Sylvia G.   Wurtz Jean-Marie   Renaud Jean-Paul   Sassone-Corsi Paolo   Lalli Enzo  

Human Molecular Genetics, Vol. 12, Iss. 9, 2003-05 ,pp. : 1063-1072

Oxford University Press

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