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Clinical Genetics|July 12, 2008
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11N Hilgert, F Alasti, N Dieltjens, et al.Clinical Genetics|July 12, 2008
Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4E Steichen-Gersdorf, I Gassner, A Superti-Furga, et al.Clinical Genetics|July 12, 2008
Attitudes antecedent to transition to self-management of a chronic genetic disorderE Giarelli, B A Bernhardt, R E PyeritzClinical Genetics|September 27, 2007
Beta-globin gene cluster polymorphisms are strongly associated with severity of HbE/beta(0)-thalassemiaQ Ma, K Abel, O Sripichai, et al.Clinical Genetics|September 20, 2007
Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in PakistanS-I Kitajiri, R McNamara, T Makishima, et al.Clinical Genetics|August 28, 2007
Cystic fibrosis in a southern Brazilian population: characteristics of 90% of the allelesF R Faucz, J Gimenez, M D Ramos, et al.Clinical Genetics|August 28, 2007
CYR61 polymorphisms are associated with plasma HDL-cholesterol levels in obese individualsL Bouchard, A Tchernof, Y Deshaies, et al.Clinical Genetics|September 1, 1991
Association of a genetic polymorphism in human apolipoprotein B-100 with intermediate density lipoprotein concentrationsM T Robinson, R Butler, R M KraussClinical Genetics|September 1, 1991
Absence of predictable phenotypic expression in proximal 15q duplicationsC J Ludowese, K J Thompson, G S Sekhon, et al.Clinical Genetics|September 1, 1991
Patients with deletions of 9q22q34 do not define a syndrome: three case reports and a literature reviewS A Farrell, J Siegel-Bartelt, I TeshimaPageof 718