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European Journal of Human Genetics : EJHG|January 13, 2011
Mitochondrial analysis of a Byzantine population reveals the differential impact of multiple historical events in South AnatoliaClaudio Ottoni, François-X Ricaut, Nancy Vanderheyden, et al.
European Journal of Human Genetics : EJHG|January 13, 2011
Evidence for RPGRIP1 gene as risk factor for primary open angle glaucomaLorena Fernández-Martínez, Stef Letteboer, Christian Y Mardin, et al.
European Journal of Human Genetics : EJHG|January 13, 2011
Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresiaMarie Cognet, Agnés Nougayrede, Valérie Malan, et al.
European Journal of Human Genetics : EJHG|December 16, 2010
Concurrent genetic alterations in DNA polymerase proofreading and mismatch repair in human colorectal cancerRintaro Yoshida, Kaname Miyashita, Mayuko Inoue, et al.
European Journal of Human Genetics : EJHG|December 15, 2010
Prevalence of CDKN2A mutations in pancreatic cancer patients: implications for genetic counselingRobert R McWilliams, Eric D Wieben, Kari G Rabe, et al.
European Journal of Human Genetics : EJHG|December 15, 2010
Relation of a common variant of the adiponectin gene to serum adiponectin concentration and metabolic traits in an aged Japanese populationDaisuke Tanimura, Rei Shibata, Hideo Izawa, et al.
European Journal of Human Genetics : EJHG|December 15, 2010
EPIBLASTER-fast exhaustive two-locus epistasis detection strategy using graphical processing unitsTony Kam-Thong, Darina Czamara, Koji Tsuda, et al.
European Journal of Human Genetics : EJHG|December 15, 2010
Distinctive microRNA expression profiles in CD34+ bone marrow cells from patients with myelodysplastic syndromeMichaela Dostalova Merkerova, Zdenek Krejcik, Hana Votavova, et al.
European Journal of Human Genetics : EJHG|January 6, 2011
An atypical case of hypomethylation at multiple imprinted lociEmma L Baple, Rebecca L Poole, Sahar Mansour, et al.
European Journal of Human Genetics : EJHG|December 24, 2010
Splicing mutations in glycogen-storage disease type II: evaluation of the full spectrum of mutations and their relation to patients' phenotypesStefania Zampieri, Emanuele Buratti, Silvia Dominissini, et al.
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