Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32

By Esparza-Gordillo Jorge  

Human Molecular Genetics, Vol. 14, Iss. 5, 2005-03 ,pp. : 703-712

Oxford University Press

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γ 2-COP , a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome

By Blagitko Nadya  

Human Molecular Genetics, Vol. 8, Iss. 13, 1999-12 ,pp. : 2387-2396

Oxford University Press

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Linkage of the Gene for the Triple A Syndrome to Chromosome 12q13 Near the Type II Keratin Gene Cluster

By Weber Angela   Wienker Thomas F.   Jung Martin   Easton Douglas   Dean Heather J.   Heinrichs Claudine   Reis Andre   Clark Adrian J. L.  

Human Molecular Genetics, Vol. 5, Iss. 12, 1996-12 ,pp. : 2061-2066

Oxford University Press

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The distribution of repressive histone modifications on silenced FMR1 alleles provides clues to the mechanism of gene silencing in fragile X syndrome

By Kumari Daman   Usdin Karen  

Human Molecular Genetics, Vol. 19, Iss. 23, 2010-12 ,pp. : 4634-4642

Oxford University Press

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A systematic gene-based screen of chr4q22q32 identifies association of a novel susceptibility gene, DKK2 , with the quantitative trait of alcohol dependence symptom counts

By Kalsi Gursharan   Kuo Po-Hsiu   Aliev Fazil   Alexander Jeffry   McMichael Omari   Patterson Diana G.   Walsh Dermot   Zhao Zhongming   Schuckit Marc   Nurnberger John   Edenberg Howard   Kramer John   Vladimirov Vladimir   Prescott Carol A.   Dick Danielle M.   Kendler Kenneth S.   Riley Brien P.  

Human Molecular Genetics, Vol. 19, Iss. 12, 2010-06 ,pp. : 2497-2506

Oxford University Press

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