Preaxial polydactyly caused by Gli3 haploinsufficiency is rescued by Zic3 loss of function in mice

By Quinn Malgorzata E.   Haaning Allison   Ware Stephanie M.  

Human Molecular Genetics, Vol. 21, Iss. 8, 2012-04 ,pp. : 1888-1896

Oxford University Press

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Zic2 -associated holoprosencephaly is caused by a transient defect in the organizer region during gastrulation

By Warr Nicholas   Powles-Glover Nicola   Chappell Anna   Robson Joan   Norris Dominic   Arkell Ruth M.  

Human Molecular Genetics, Vol. 17, Iss. 19, 2008-10 ,pp. : 2986-2996

Oxford University Press

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In vitro analysis of partial loss-of-function ZIC2 mutations in holoprosencephaly: alanine tract expansion modulates DNA binding and transactivation

By Brown Lucia   Paraso Melinda   Brown Stephen  

Human Molecular Genetics, Vol. 14, Iss. 3, 2005-02 ,pp. : 411-420

Oxford University Press

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Holoprosencephaly due to mutations in ZIC2 : alanine tract expansion mutations may be caused by parental somatic recombination

By Sommer A.  

Human Molecular Genetics, Vol. 10, Iss. 8, 2001-04 ,pp. : 791-796

Oxford University Press

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Changing Faces of Transcriptional Regulation Reflected by Zic3

By  

Current Genomics, Vol. 16, Iss. 2, 2015-04 ,pp. : 117-127

Bentham Science Publishers

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