A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate

By Chatterjee K.  

Human Molecular Genetics, Vol. 11, Iss. 17, 2002-06 ,pp. : 2051-2059

Oxford University Press

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Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate

By Chiquet Brett T.   Blanton Susan H.   Burt Amber   Ma Deqiong   Stal Samuel   Mulliken John B.   Hecht Jacqueline T.  

Human Molecular Genetics, Vol. 17, Iss. 14, 2008-07 ,pp. : 2212-2218

Oxford University Press

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Mutation Analysis of FOXF2 in Patients with Disorders of Sex Development (DSD) in Combination with Cleft Palate

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Sexual Development, Vol. 2, Iss. 6, 2009-03 ,pp. : 302-308

Karger

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Characterization of lpd (lipid defect): a novel mutation on mouse chromosome 16 associated with a defect in triglyceride metabolism

By Wen X-Y.   Bryce D.M.   Breitman M.L.  

Human Molecular Genetics, Vol. 7, Iss. 4, 1998-04 ,pp. : 743-750

Oxford University Press

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PHF8 , a gene associated with cleft lip/palate and mental retardation, encodes for an N ε -dimethyl lysine demethylase

By Loenarz Christoph   Ge Wei   Coleman Mathew L.   Rose Nathan R.   Cooper Christopher D.O.   Klose Robert J.   Ratcliffe Peter J.   Schofield Christopher J.  

Human Molecular Genetics, Vol. 19, Iss. 2, 2010-01 ,pp. : 217-222

Oxford University Press

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