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Journal of Medical Genetics|January 1, 1997
Fragile X syndrome is less common than previously estimatedJ E Morton, S Bundey, T P Webb, et al.Journal of Medical Genetics|January 1, 1997
No evidence for uniparental disomy as a common cause of Sotos syndromeM Smith, P Fullwood, Y Qi, et al.Journal of Medical Genetics|January 1, 1997
Polymorphic markers of the glycogen debranching enzyme gene allowing linkage analysis in families with glycogen storage disease type IIIJ Shen, H M Liu, Y Bao, et al.Journal of Medical Genetics|January 1, 1997
Germline HNPCC gene variants have little influence on the risk for sporadic colorectal cancerI P Tomlinson, N E Beck, T Homfray, et al.Journal of Medical Genetics|January 1, 1997
Down syndrome: characterisation of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21) (q26;q22.1) by FISHM Nadal, S Moreno, M Pritchard, et al.Journal of Medical Genetics|January 1, 1997
Gaucher disease: molecular screening of the glucocerebrosidase 1601G and 1601A alleles in Victoria, British Columbia, CanadaF Y Choy, J Linsey, P D MacLeodJournal of Medical Genetics|October 1, 1996
Mutation analysis of the BRCA1 gene in 23 families with cases of cancer of the breast, ovary, and multiple other sitesF Durocher, P Tonin, D Shattuck-Eidens, et al.Journal of Medical Genetics|October 1, 1996
Adverse psychological events occurring in the first year after predictive testing for Huntington's disease. The Canadian Collaborative Study Predictive TestingK Lawson, S Wiggins, T Green, et al.Journal of Medical Genetics|October 1, 1996
Megalocornea-mental retardation syndrome: report of a new caseI Barisić, I Ligutić, L ZergollernJournal of Medical Genetics|September 1, 1996
Mutation screening of MSH2 and MLH1 mRNA in hereditary non-polyposis colon cancer syndromeN J Froggatt, C Brassett, D J Koch, et al.Pageof 649