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Clinical Genetics|October 27, 1998
Three novel PROC gene lesions causing protein C deficiencyP J Hallam, P Mannucci, A Tripodi, et al.Clinical Genetics|July 1, 1993
Craniofacial anthropometric studies in Waardenburg syndrome type IE O da-Silva, J E Batista, M A Medeiros, et al.Clinical Genetics|March 1, 1993
Normal immunological status in four patients with ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC-syndrome)N Obel, B Hansen, F T BlackClinical Genetics|January 1, 1997
The role of the apolipoprotein E polymorphism in the prediction of coronary artery disease age of onsetJ H Moore, S L Reilly, R E Ferrell, et al.Clinical Genetics|January 1, 1997
An autosomal recessive adducted thumb-club foot syndrome observed in Turkish cousinsM Dundar, F Demiryilmaz, I Demiryilmaz, et al.Clinical Genetics|January 1, 1997
Chromosome deletion 17p11.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigationF Behjati, M Mullarkey, A Bergbaum, et al.Clinical Genetics|April 1, 1996
A G-1-to-A acceptor splice site LDLR mutant allele leads to reduced relative transcript levels in patients with heterozygous familial hypercholesterolemiaH K Jensen, L G Jensen, P S Hansen, et al.Clinical Genetics|April 1, 1996
Two novel mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in a Spanish populationA Cenarro, H K Jensen, F Civeira, et al.Clinical Genetics|April 1, 1996
De novo 46,XX, dir dup (11)(q133.3-->q14.2) in a patient with mental retardation, congenital cardiopathy and thrombopeniaE Legius, I Wlodarska, L Selleri, et al.Pageof 719