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Lancet (London, England)|October 16, 1993
Molecular analysis and clinical correlations of the Huntington's disease mutationJ C MacMillan, R G Snell, A Tyler, et al.Human Genetics|January 1, 1985
Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophyC S Brown, N S Thomas, M Sarfarazi, et al.American Journal of Human Genetics|July 1, 1991
Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA markerH G Harley, J D Brook, J Floyd, et al.Genomics|November 1, 1988
Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locusH G Harley, J D Brook, C L Jackson, et al.British Journal of Anaesthesia|December 5, 2000
Within-breath arterial PO2 oscillations in an experimental model of acute respiratory distress syndromeE M Williams, J P Viale, R M Hamilton, et al.Case Reports in Obstetrics and Gynecology|March 17, 2017
Can Surgery Be Avoided? Exclusive Antibiotic Treatment for Pelvic ActinomycosisM P Ruiz, E M Williams, C M Markey, et al.Human Genetics|November 1, 1986
Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19D J Shaw, A L Meredith, M Sarfarazi, et al.Current Biology : CB|October 13, 1998
Dynamics and ultrastructure of developmental cell fusions in the Caenorhabditis elegans hypodermisW A Mohler, J S Simske, E M Williams-Masson, et al.American Journal of Human Genetics|March 1, 1991
Assignment of Emery-Dreifuss muscular dystrophy to the distal region of Xq28: the results of a collaborative studyG G Consalez, N S Thomas, C L Stayton, et al.American Journal of Human Genetics|June 1, 1993
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophyH G Harley, S A Rundle, J C MacMillan, et al.Pageof 30