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European Journal of Human Genetics : EJHG|May 25, 2006
Genetics and pathophysiology of mental retardationJamel Chelly, Malik Khelfaoui, Fiona Francis, et al.
European Journal of Human Genetics : EJHG|May 25, 2006
The genetic basis of emotional behaviour in miceSaffron A G Willis-Owen, Jonathan Flint
European Journal of Human Genetics : EJHG|May 25, 2006
Molecular genetics of the fruit-fly circadian clockEzio Rosato, Eran Tauber, Charalambos P Kyriacou
European Journal of Human Genetics : EJHG|August 23, 2007
Attitudes regarding carrier testing in incompetent children: a survey of European clinical geneticistsPascal Borry, Tom Goffin, Herman Nys, et al.
European Journal of Human Genetics : EJHG|August 23, 2007
New genetic evidence supports isolation and drift in the Ladin communities of the South Tyrolean Alps but not an ancient origin in the Middle EastMark G Thomas, Ian Barnes, Michael E Weale, et al.
European Journal of Human Genetics : EJHG|July 27, 2007
Two-stage association tests for genome-wide association studies based on family data with arbitrary family structureTao Feng, Shuanglin Zhang, Qiuying Sha
European Journal of Human Genetics : EJHG|June 26, 2008
Predicting the number and sizes of IBD regions among family members and evaluating the family size requirement for linkage studiesWanling Yang, Zhanyong Wang, Lusheng Wang, et al.
European Journal of Human Genetics : EJHG|October 13, 2006
A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardationIsabel Martínez-Garay, Miguel Tomás, Silvestre Oltra, et al.
European Journal of Human Genetics : EJHG|December 7, 2006
Genetic screening for autosomal recessive nonsyndromic mental retardation in an isolated population in IsraelLina Basel-Vanagaite, Ellen Taub, Gabrielle J Halpern, et al.
European Journal of Human Genetics : EJHG|February 19, 2004
Complete germline deletion of the STK11 gene in a family with Peutz-Jeghers syndromeNathalie Le Meur, Cosette Martin, Pascale Saugier-Veber, et al.
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