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European Journal of Human Genetics : EJHG|March 16, 2007
A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermiaEva Morava, Renate Zeevaert, Eckhard Korsch, et al.
European Journal of Human Genetics : EJHG|March 16, 2007
A legal framework for biobanking: the German experienceJürgen Simon, Rainer Paslack, Jürgen Robienski, et al.
European Journal of Human Genetics : EJHG|November 16, 2006
Autozygosity mapping of Bardet-Biedl syndrome to 12q21.2 and confirmation of FLJ23560 as BBS10Dominic R A White, Anuradha Ganesh, Darryl Nishimura, et al.
European Journal of Human Genetics : EJHG|October 13, 2006
Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approachJürgen Tomiuk, Lutz Bachmann, Claudia Bauer, et al.
European Journal of Human Genetics : EJHG|December 14, 2006
Methods for the selection of tagging SNPs: a comparison of tagging efficiency and performanceKeyue Ding, Iftikhar J Kullo
European Journal of Human Genetics : EJHG|January 5, 2007
Significant variation in haplotype block structure but conservation in tagSNP patterns among global populationsSheng Gu, Andrew J Pakstis, Hui Li, et al.
European Journal of Human Genetics : EJHG|August 19, 2007
Co-introgression of Y-chromosome haplogroups and the sickle cell gene across Africa's SahelRihab E Bereir, Hisham Y Hassan, Niven A Salih, et al.
European Journal of Human Genetics : EJHG|August 9, 2007
Population history and infrequent mutations: how old is a rare mutation? GUCY2D as a worked exampleSylvain Hanein, Isabelle Perrault, Sylvie Gerber, et al.
European Journal of Human Genetics : EJHG|July 20, 2007
Risk estimation for familial breast cancer: improving the system of counsellingHelen Gregory, Sarah Wordsworth, Barbara Gibbons, et al.
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