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European Journal of Human Genetics : EJHG|October 8, 2015
Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery, Ivan Eisler, Matthew Ellison, et al.European Journal of Human Genetics : EJHG|October 22, 2015
Genetic evidence for an origin of the Armenians from Bronze Age mixing of multiple populationsMarc Haber, Massimo Mezzavilla, Yali Xue, et al.European Journal of Human Genetics : EJHG|October 22, 2015
West syndrome caused by homozygous variant in the evolutionary conserved gene encoding the mitochondrial elongation factor GUF1Ali Abdullah Alfaiz, Verena Müller, Nadia Boutry-Kryza, et al.European Journal of Human Genetics : EJHG|October 22, 2015
De novo dominant variants affecting the motor domain of KIF1A are a cause of PEHO syndromeSylvie Langlois, Maja Tarailo-Graovac, Bryan Sayson, et al.European Journal of Human Genetics : EJHG|December 11, 2014
Challenges and solutions for gene identification in the presence of familial locus heterogeneityAtteeq U Rehman, Regie Lyn P Santos-Cortez, Meghan C Drummond, et al.European Journal of Human Genetics : EJHG|April 7, 2016
A novel kinase mutation in VEGFR-1 predisposes its αC-helix/activation loop towards allosteric activation: Atomic insights from protein simulationTaseem A Mokhdomi, Shoiab Bukhari, Naveed Anjum Chikan, et al.European Journal of Human Genetics : EJHG|March 17, 2016
CAG repeat size in Huntingtin alleles is associated with cancer prognosisMorgane Sonia Thion, Sophie Tézenas du Montcel, Jean-Louis Golmard, et al.European Journal of Human Genetics : EJHG|April 14, 2016
Unsolicited findings of next-generation sequencing for tumor analysis within a Dutch consortium: clinical daily practice reconsideredRhodé M Bijlsma, Annelien L Bredenoord, Christa G Gadellaa-Hooijdonk, et al.European Journal of Human Genetics : EJHG|April 14, 2016
Nucleoporin genes in human diseasesValeria Nofrini, Danika Di Giacomo, Cristina MecucciEuropean Journal of Human Genetics : EJHG|August 20, 2015
The more the merrier? How a few SNPs predict pigmentation phenotypes in the Northern German populationAmke Caliebe, Melanie Harder, Rebecca Schuett, et al.Pageof 564