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Human Genetics|October 1, 1986
Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome)K D MacDermot, R M Winter, S MalcolmJournal of Medical Genetics|August 1, 1986
Robinow syndrome without mesomelic 'brachymelia': a report of five casesM D Bain, R M Winter, J BurnJournal of Medical Genetics|April 1, 1984
A computerised data base for the diagnosis of rare dysmorphic syndromesR M Winter, M Baraitser, J M DouglasJournal of Medical Genetics|February 1, 1986
A case of Fryns syndromeI D Young, K Simpson, R M WinterJournal of Medical Genetics|December 1, 1989
Unknown syndrome: pachygyria, joint contractures, and facial abnormalitiesR M Winter, B N Harding, J HydeClinical Dysmorphology|October 1, 1993
Kivlin syndrome and Peters'-Plus syndrome: are they the same disorder?E M Thompson, R M Winter, M BaraitserClinical Genetics|October 1, 1983
Greig cephalopolysyndactyly: report of 13 affected individuals in three familiesM Baraitser, R M Winter, E M BrettAnnals of Human Genetics|February 20, 2002
Nonsyndromic cleft lip and palate: complex genetics and environmental effectsN J Prescott, R M Winter, S MalcolmJournal of Medical Genetics|April 1, 1990
Ellis-van creveld syndrome, Jeune syndrome, and renal-hepatic-pancreatic dysplasia: separate entities or disease spectrum?L A Brueton, M J Dillon, R M WinterAmerican Journal of Medical Genetics|August 1, 1985
A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardationM E Pembrey, R M Winter, K E DaviesPageof 19