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Journal of Medical Genetics|August 1, 1983
Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosomeH M Kingston, N S Thomas, P L Pearson, et al.American Journal of Human Genetics|January 1, 1989
Close flanking markers for neurofibromatosis type I (NF1)M Upadhyaya, M Sarfarazi, S M Huson, et al.Archives of Disease in Childhood|April 1, 1992
Anal abnormalities in childhood myotonic dystrophy--a possible source of confusion in child sexual abuseW Reardon, H E Hughes, S H Green, et al.The Journal of Pediatrics|March 1, 1989
Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysisJ Zonana, M Sarfarazi, N S Thomas, et al.The Quarterly Journal of Medicine|June 1, 1991
Polycystic kidney disease re-evaluated: a population-based studyF Davies, G A Coles, P S Harper, et al.Prenatal Diagnosis|September 1, 1990
Chorionic villus sampling for prenatal diagnosis in Wales using DNA probes--5 years' experienceM Upadhyaya, A Fryer, G Foat, et al.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.Pageof 23