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Journal of Medical Genetics|January 1, 1989
Congenital hypothyroidism, spiky hair, and cleft palateJ S Bamforth, I A Hughes, J H Lazarus, et al.Human Genetics|May 1, 1989
Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19M Koch, H Harley, M Sarfarazi, et al.Journal of Medical Genetics|December 1, 1986
Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studiesA Clarke, S H Roberts, N S Thomas, et al.Human Molecular Genetics|April 1, 1996
Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brainJ D Wood, J C MacMillan, P S Harper, et al.Lancet (London, England)|June 6, 1987
Exclusion testing for Huntington's disease in pregnancy with a closely linked DNA markerO W Quarrell, A L Meredith, A Tyler, et al.Journal of Medical Genetics|August 1, 1983
The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophyP S Harper, T O'Brien, J M Murray, et al.Clinical Genetics|November 1, 1982
Mannosidosis in two brothers: prolonged survival in the severe phenotypeM A Patton, I C Barnes, I D Young, et al.Age and Ageing|November 1, 1994
Late-onset Huntington's disease: a clinical and molecular studyC M James, G D Houlihan, R G Snell, et al.Journal of Medical Genetics|August 1, 1983
Absence of genetic heterogeneity in Duchenne muscular dystrophy shown by a linkage study using two cloned DNA sequencesT O'Brien, P S Harper, K E Davies, et al.American Journal of Medical Genetics|January 1, 1990
Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysisJ Zonana, A Schinzel, M Upadhyaya, et al.Pageof 30