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European Journal of Human Genetics : EJHG|August 26, 2010
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairmentNicola Brunetti-Pierri, Alex R Paciorkowski, Roberto Ciccone, et al.
European Journal of Human Genetics : EJHG|August 26, 2010
A major Y-chromosome haplogroup R1b Holocene era founder effect in Central and Western EuropeNatalie M Myres, Siiri Rootsi, Alice A Lin, et al.
European Journal of Human Genetics : EJHG|June 1, 2010
New RAB3GAP1 mutations in patients with Warburg Micro Syndrome from different ethnic backgrounds and a possible founder effect in the DanishDeborah J Morris-Rosendahl, Reeval Segel, A Peter Born, et al.
European Journal of Human Genetics : EJHG|September 30, 2010
The Y-chromosome landscape of the Philippines: extensive heterogeneity and varying genetic affinities of Negrito and non-Negrito groupsFrederick Delfin, Jazelyn M Salvador, Gayvelline C Calacal, et al.
European Journal of Human Genetics : EJHG|June 24, 2010
Genes predict village of origin in rural EuropeColm O'Dushlaine, Ruth McQuillan, Michael E Weale, et al.
European Journal of Human Genetics : EJHG|June 24, 2010
Population structure and genome-wide patterns of variation in Ireland and BritainColm T O'Dushlaine, Derek Morris, Valentina Moskvina, et al.
European Journal of Human Genetics : EJHG|June 17, 2010
Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenaseAviva Levitas, Emad Muhammad, Gali Harel, et al.
European Journal of Human Genetics : EJHG|December 2, 2010
Mutation in subdomain G' of mitochondrial elongation factor G1 is associated with combined OXPHOS deficiency in fibroblasts but not in musclePaulien Smits, Hana Antonicka, Peter M van Hasselt, et al.
European Journal of Human Genetics : EJHG|December 2, 2010
A population-based study of polymorphisms in genes related to sex hormones and abdominal aortic aneurysmJonathan Golledge, Erik Biros, Nicole Warrington, et al.
European Journal of Human Genetics : EJHG|January 22, 2009
Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocentesesAntonino Forabosco, Antonio Percesepe, Sandra Santucci
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