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By Grehan N.  

Human Molecular Genetics, Vol. 12, Iss. 5, 2003-03 ,pp. : 575-582

Oxford University Press

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Functional genetic analysis of mutations implicated in a human speech and language disorder

By Vernes Sonja C.   Nicod Jérôme   Coventry Julie A.   Kenny Niamh   Coupe Anne-Marie   Bird Louise E.   Davies Kay E.   Fisher Simon E.  

Human Molecular Genetics, Vol. 15, Iss. 21, 2006-11 ,pp. : 3154-3167

Oxford University Press

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Functional analysis of cone–rod homeobox (CRX) mutations associated with retinal dystrophy

By Chen S.  

Human Molecular Genetics, Vol. 11, Iss. 8, 2002-04 ,pp. : 873-884

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Functional Analysis of Novel Androgen Receptor Mutations in a Unique Cohort of Indonesian Patients with a Disorder of Sex Development

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Sexual Development, Vol. 3, Iss. 5, 2009-10 ,pp. : 237-244

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Naturally occurring germline and tumor-associated mutations within the ATP-binding motifs of PTEN lead to oxidative damage of DNA associated with decreased nuclear p53

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Human Molecular Genetics, Vol. 20, Iss. 1, 2011-01 ,pp. : 80-89

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