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Clinical Genetics|June 30, 2009
Hepatic lipase promoter C-480T polymorphism is associated with serum lipids levels, but not subclinical atherosclerosis: the Cardiovascular Risk in Young Finns StudyY-M Fan, O T Raitakari, M Kähönen, et al.Clinical Genetics|January 28, 2009
Toriello-Carey syndrome in a patient with a de novo balanced translocation [46,XY,t(2;14)(q33;q22)] interrupting SATB2D H Tegay, K K Chan, L Leung, et al.Clinical Genetics|July 1, 1991
Identification of the 664 proline to leucine mutation in the low density lipoprotein receptor in four unrelated patients with familial hypercholesterolaemia in the UKL King-Underwood, V Gudnason, S Humphries, et al.Clinical Genetics|July 1, 1991
Germinal mosaicism in Crouzon syndrome. A family with three affected siblings of normal parentsC Navarrete, R Peña, R Peñaloza, et al.Clinical Genetics|July 1, 1991
A simplified protocol for fluorescence in situ hybridization with repetitive DNA probes and its use in clinical cytogeneticsO Bartsch, E SchwingerClinical Genetics|December 5, 2008
Preimplantation genetic diagnosis in an HIV-serodiscordant couple carrier for sickle cell disease: lessons from a case reportE Gonzalez-Merino, V Zengbe, A S Vannin, et al.Clinical Genetics|November 22, 2008
Estrogen receptor status in CHEK2-positive breast cancers: implications for chemopreventionC Cybulski, T Huzarski, T Byrski, et al.Clinical Genetics|November 22, 2008
Congenital gastrointestinal defects in Down syndrome: a report from the Atlanta and National Down Syndrome ProjectsS B Freeman, C P Torfs, P A Romitti, et al.Clinical Genetics|November 22, 2008
The impact of familial environment on depression scores after genetic testing for cancer susceptibilityS Ashida, D W Hadley, B K Vaughn, et al.Pageof 718