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Clinical Genetics|June 1, 1991
Prenatal diagnosis of lethal osteogenesis imperfecta in twin pregnancyL R Morin, M Herlicoviez, J C Loisel, et al.Clinical Genetics|September 2, 2008
Spectrum of novel mutations in the human PKLR gene in pyruvate kinase-deficient Indian patients with heterogeneous clinical phenotypesP Kedar, T Hamada, P Warang, et al.Clinical Genetics|August 15, 2008
Multiplex MassARRAY spectrometry (iPLEX) produces a fast and economical test for 56 familial hypercholesterolaemia-causing mutationsW T Wright, S V Heggarty, I S Young, et al.Clinical Genetics|August 16, 2005
'Indirect' BRCA1/2 testing: a useful approach in hereditary breast and ovarian cancer families without a living affected relativeD G Cruger, T A Kruse, A M GerdesClinical Genetics|August 16, 2005
A novel locus for autosomal dominant hereditary gingival fibromatosis, GINGF3, maps to chromosome 2p22.3-p23.3X Ye, L Shi, Y Cheng, et al.Clinical Genetics|August 16, 2005
An exploratory comparison of genetic counselling protocols for HNPCC predictive testingK Brain, S Sivell, K Bennert, et al.Clinical Genetics|August 16, 2005
Association of repeat polymorphisms in the estrogen receptors alpha, beta, and androgen receptor genes with knee osteoarthritisP Fytili, E Giannatou, V Papanikolaou, et al.Clinical Genetics|January 6, 2007
Diagnosis and management of early- and late-onset cerebellar ataxiaE Brusse, J A Maat-Kievit, J C van SwietenClinical Genetics|January 6, 2007
The correlation of CTG repeat length with material and social deprivation in myotonic dystrophyL Laberge, S Veillette, J Mathieu, et al.Pageof 718