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Human Molecular Genetics, Vol. 20, Iss. 7, 2011-04 ,pp. : 1306-1314

Oxford University Press

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Biochemical analysis of pathogenic ligand-dependent FGFR2 mutations suggests distinct pathophysiological mechanisms for craniofacial and limb abnormalities

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Human Molecular Genetics, Vol. 13, Iss. 19, 2004-10 ,pp. : 2313-2324

Oxford University Press

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Novel VANGL1 Gene Mutations in 144 Slovakian, Romanian and German Patients with Neural Tube Defects

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Molecular Syndromology, Vol. 3, Iss. 2, 2012-07 ,pp. : 76-81

Karger

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Skeletal muscle repair in a mouse model of nemaline myopathy

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Human Molecular Genetics, Vol. 15, Iss. 17, 2006-09 ,pp. : 2603-2612

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Cardiovascular defects in a mouse model of HOXA1 syndrome

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Human Molecular Genetics, Vol. 21, Iss. 1, 2012-01 ,pp. : 26-31

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