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European Journal of Human Genetics : EJHG|April 12, 2007
Abundance of the POLG disease mutations in Europe, Australia, New Zealand, and the United States explained by single ancient European foundersAnna H Hakonen, Guido Davidzon, Renato Salemi, et al.
European Journal of Human Genetics : EJHG|March 8, 2007
Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletionJeroen Knijnenburg, Arie van Haeringen, Kerstin B M Hansson, et al.
European Journal of Human Genetics : EJHG|March 8, 2007
Genetic component of identification, intensity and pleasantness of odours: a Finnish family studyAntti Knaapila, Kaisu Keskitalo, Mikko Kallela, et al.
European Journal of Human Genetics : EJHG|March 8, 2007
Angioma serpiginosum with oesophageal papillomatosis is an X-linked dominant condition that maps to Xp11.3-Xq12Ellen O Blinkenberg, Atle Brendehaug, Arne K Sandvik, et al.
European Journal of Human Genetics : EJHG|June 15, 2007
Genotype-phenotype correlations in 19 Dutch cases with APC gene deletions and a literature reviewMaartje Nielsen, Elsa Bik, Frederik J Hes, et al.
European Journal of Human Genetics : EJHG|December 14, 2006
Functional analysis of human S-adenosylhomocysteine hydrolase isoforms SAHH-2 and SAHH-3Ksenija Fumić, Robert Beluzić, Mario Cuk, et al.
European Journal of Human Genetics : EJHG|June 28, 2007
Polymorphism of XRCC1 predicts overall survival of gastric cancer patients receiving oxaliplatin-based chemotherapy in Chinese populationBaorui Liu, Jia Wei, Zhengyun Zou, et al.
European Journal of Human Genetics : EJHG|July 5, 2007
Process and outcome in communication of genetic information within families: a systematic reviewClara L Gaff, Angus J Clarke, Paul Atkinson, et al.
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