Mutations in the human melanocortin-4 receptor gene associated with severe familial obesity disrupts receptor function through multiple molecular mechanisms

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Human Molecular Genetics, Vol. 12, Iss. 5, 2003-03 ,pp. : 561-574

Oxford University Press

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Disruption of the Clathrin Heavy Chain-Like Gene ( CLTCL ) Associated with Features of DGS/VCFS: A Balanced (21;22)(p12;q11) Translocation

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Human Molecular Genetics, Vol. 6, Iss. 3, 1997-01 ,pp. : 357-367

Oxford University Press

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Sim1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamus

By Himms-Hagen J.  

Human Molecular Genetics, Vol. 10, Iss. 14, 2001-07 ,pp. : 1465-1473

Oxford University Press

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Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss

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Molecular Syndromology, Vol. 5, Iss. 1, 2013-10 ,pp. : 3-10

Karger

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Epigenetic loss of the familial tumor-suppressor gene exostosin-1 (EXT1) disrupts heparan sulfate synthesis in cancer cells

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Human Molecular Genetics, Vol. 13, Iss. 22, 2004-11 ,pp. : 2753-2765

Oxford University Press

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