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Journal of Medical Genetics|December 1, 1979
Partial monosomy 7 with interstitial deletions in two infants with differing congenital abnormalitiesM D Crawfurd, I Kessel, M Liberman, et al.Cancer Genetics and Cytogenetics|March 1, 1989
Translocation 1;7 in four cases of myeloid disordersD M Sheppard, K E Richkind, M BullCancer Genetics and Cytogenetics|February 1, 1988
Karyotypic analysis of the human monoblastic cell line U937J M Shipley, D M Sheppard, D SheerCancer Genetics and Cytogenetics|April 1, 1985
Karyotypic analysis and chromosome polymorphisms in four choriocarcinoma cell linesD M Sheppard, R A Fisher, S D LawlerBritish Medical Journal (Clinical Research Ed.)|April 24, 1982
Twin pregnancy with complete hydatidiform mole (46,XX) and fetus (46,XY): genetic origin proved by analysis of chromosome polymorphismsR A Fisher, D M Sheppard, S D LawlerBritish Journal of Obstetrics and Gynaecology|July 1, 1984
Two patients with complete hydatidiform mole with 46,XY karyotypeR A Fisher, D M Sheppard, S D LawlerThe Biochemical Journal|October 1, 1983
Purification of uroporphyrinogen decarboxylase from human erythrocytes. Immunochemical evidence for a single protein with decarboxylase activity in human erythrocytes and liverG H Elder, J A Tovey, D M SheppardThe Quarterly Journal of Medicine|January 1, 1981
A newly recognized syndrome of connective tissue dysplasia in siblings (previously described as a variant of Morquio disease)E Spellacy, D A Gibbs, R W WattsClinica Chimica Acta; International Journal of Clinical Chemistry|June 30, 1983
Studies on the composition of urinary glycosaminoglycans and oligosaccharides in patients with mucopolysaccharidoses who were receiving fibroblast transplantsP Purkiss, D A Gibbs, R W WattsNeuropsychologia|October 31, 2001
Abnormal line bisection judgements in children with Tourette's syndromeD M Sheppard, J L Bradshaw, J B MattingleyPageof 5