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European Journal of Human Genetics : EJHG|August 2, 2007
Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHDBarbara Pasini, Sarah R McWhinney, Thalia Bei, et al.European Journal of Human Genetics : EJHG|July 5, 2007
Genetic analysis of the GRM1 gene in human melanoma susceptibilityPablo Ortiz, Francisco Vanaclocha, Eduardo López-Bran, et al.European Journal of Human Genetics : EJHG|July 5, 2007
A sensitive assay for measuring SMN mRNA levels in peripheral blood and in muscle samples of patients affected with spinal muscular atrophyMyriam Vezain, Pascale Saugier-Veber, Judith Melki, et al.European Journal of Human Genetics : EJHG|July 27, 2006
DISCERN-Genetics: quality criteria for information on genetic testingSasha Shepperd, Peter Farndon, Vivian Grainge, et al.European Journal of Human Genetics : EJHG|July 27, 2006
The emergence of an ethical duty to disclose genetic research results: international perspectivesBartha Maria Knoppers, Yann Joly, Jacques Simard, et al.European Journal of Human Genetics : EJHG|July 27, 2006
A test of homogeneity of Hardy-Weinberg disequilibrium across strataXiao-Lin Yin, Wen-Qing Ma, Man-Lai Tang, et al.European Journal of Human Genetics : EJHG|June 23, 2006
Association of a 31 bp VNTR in the CBS gene with postload homocysteine concentrations in the Framingham Offspring StudyKarin J A Lievers, Leo A J Kluijtmans, Henk J Blom, et al.European Journal of Human Genetics : EJHG|June 15, 2006
TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletionsLiesbeth Rooms, Edwin Reyniers, Stefaan Scheers, et al.European Journal of Human Genetics : EJHG|June 15, 2006
A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairmentNanna D Rendtorff, Mei Zhu, Toril Fagerheim, et al.Pageof 564