Comparative gene expression analysis of avian embryonic facial structures reveals new candidates for human craniofacial disorders

By Brugmann S.A.   Powder K.E.   Young N.M.   Goodnough L.H.   Hahn S.M.   James A.W.   Helms J.A.   Lovett M.  

Human Molecular Genetics, Vol. 19, Iss. 5, 2010-03 ,pp. : 920-930

Oxford University Press

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Human SULT1A1 gene: copy number differences and functional implications

By Hebbring Scott J.   Adjei Araba A.   Baer Janel L.   Jenkins Gregory D.   Zhang Jianping   Cunningham Julie M.   Schaid Daniel J.   Weinshilboum Richard M.   Thibodeau Stephen N.  

Human Molecular Genetics, Vol. 16, Iss. 5, 2007-03 ,pp. : 463-470

Oxford University Press

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Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6

By Mitchem K.L.  

Human Molecular Genetics, Vol. 11, Iss. 16, 2002-08 ,pp. : 1887-1898

Oxford University Press

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Expression of the Ceruloplasmin Gene in the Human Retina and Brain: Implications for a Pathogenic Model in Aceruloplasminemia

By Klomp Leo W. J.   Gitlin Jonathan D.  

Human Molecular Genetics, Vol. 5, Iss. 12, 1996-12 ,pp. : 1989-1996

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Eya1 gene dosage critically affects the development of sensory epithelia in the mammalian inner ear

By Zou Dan   Erickson Christopher   Kim Eun-Hee   Jin Dongzhu   Fritzsch Bernd   Xu Pin-Xian  

Human Molecular Genetics, Vol. 17, Iss. 21, 2008-11 ,pp. : 3340-3356

Oxford University Press

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