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European Journal of Human Genetics : EJHG|December 4, 2008
A 15q13.3 microdeletion segregating with autismAlistair T Pagnamenta, Kirsty Wing, Elham Sadighi Akha, et al.
European Journal of Human Genetics : EJHG|November 27, 2008
The expression of type III hyperlipoproteinemia: involvement of lipolysis genesPeter Henneman, Femke van der Sman-de Beer, Payman Hanifi Moghaddam, et al.
European Journal of Human Genetics : EJHG|November 13, 2008
GENESTAT: an information portal for design and analysis of genetic association studiesSamuli Ripatti, Tim Becker, Heike Bickeböller, et al.
European Journal of Human Genetics : EJHG|November 6, 2008
Kallmann syndromeCatherine Dodé, Jean-Pierre Hardelin
European Journal of Human Genetics : EJHG|June 25, 2009
Comparing population structure as inferred from genealogical versus genetic informationVincenza Colonna, Teresa Nutile, Ronald R Ferrucci, et al.
European Journal of Human Genetics : EJHG|April 16, 2009
Risk-reducing surgery for ovarian cancer: outcomes in 300 surgeries suggest a low peritoneal primary riskD Gareth R Evans, Richard Clayton, Paul Donnai, et al.
European Journal of Human Genetics : EJHG|July 9, 2009
A comprehensive approach to haplotype-specific analysis by penalized likelihoodJung-Ying Tzeng, Howard D Bondell
European Journal of Human Genetics : EJHG|July 9, 2009
The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational familyErik F Hensen, Jeroen C Jansen, Maaike D Siemers, et al.
European Journal of Human Genetics : EJHG|May 21, 2009
Homozygosity for a null allele of COL3A1 results in recessive Ehlers-Danlos syndromeAurélie Plancke, Muriel Holder-Espinasse, Valérie Rigau, et al.
European Journal of Human Genetics : EJHG|February 20, 2009
A large-scale mutation search reveals genetic heterogeneity in 3M syndromeCéline Huber, Anee-Lise Delezoide, Fabien Guimiot, et al.
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