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American Journal of Human Genetics|March 6, 2012
Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFBAndreas Zankl, Emma L Duncan, Paul J Leo, et al.
European Journal of Human Genetics : EJHG|January 9, 2014
Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum: a registry-based study in EuropeIngeborg Barisic, Ljubica Odak, Maria Loane, et al.
Journal of Human Genetics|July 25, 2008
Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndromeYoko Narumi, Yoko Aoki, Tetsuya Niihori, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 19, 2014
Seasonality of congenital anomalies in EuropeJohannes Michiel Luteijn, Helen Dolk, Marie-Claude Addor, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 16, 2016
Use of hierarchical models to analyze European trends in congenital anomaly prevalenceAlana Cavadino, David Prieto-Merino, Marie-Claude Addor, et al.
British Journal of Clinical Pharmacology|June 30, 2016
EUROmediCAT signal detection: a systematic method for identifying potential teratogenic medicationJohannes M Luteijn, Joan K Morris, Ester Garne, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|August 31, 2012
Epidemiology of small intestinal atresia in Europe: a register-based studyKate E Best, Peter W G Tennant, Marie-Claude Addor, et al.
Acta Neuropathologica Communications|July 26, 2014
Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephalyCatherine Fallet-Bianco, Annie Laquerrière, Karine Poirier, et al.
Drug Safety|December 13, 2017
Beta-Blocker Use in Pregnancy and Risk of Specific Congenital Anomalies: A European Case-Malformed Control StudyJorieke E H Bergman, L Renée Lutke, Rijk O B Gans, et al.
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