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American Journal of Medical Genetics|December 1, 1987
A syndrome of mental retardation, short stature, hemolytic anemia, delayed puberty, and abnormal facial appearance: similarities to a report of aldolase A deficiencyJ A Hurst, M Baraitser, R M WinterAmerican Journal of Medical Genetics|July 1, 1985
Osteodysplastic primordial dwarfism: report of a further patient with manifestations similar to those seen in patients with types I and IIIR M Winter, J Wigglesworth, B N HardingAmerican Journal of Medical Genetics|January 1, 1988
Distinctive syndrome of short stature, craniosynostosis, skeletal changes, and malformed earsJ A Hurst, R M Winter, M BaraitserHuman 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 BrettPageof 23