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Clinical Dysmorphology|October 1, 1993
Kivlin syndrome and Peters'-Plus syndrome: are they the same disorder?E M Thompson, R M Winter, M BaraitserClinical Dysmorphology|October 1, 1993
Craniofrontonasal dysplasia in two male sibsU Natarajan, M Baraitser, K Nicolaides, et al.British Medical Journal (Clinical Research Ed.)|January 22, 1983
Effect of genetic counselling on the prevalence of Huntington's choreaC O Carter, K A Evans, M BaraitserClinical Dysmorphology|January 1, 1996
Two brothers with deafness, femoral epiphyseal dysplasia, short stature and developmental delayL S Chitty, C M Hall, M BaraitserClinical Genetics|October 1, 1983
Greig cephalopolysyndactyly: report of 13 affected individuals in three familiesM Baraitser, R M Winter, E M BrettClinical Genetics|August 1, 1988
Genetic counselling in hypomelanosis of Ito: case report and reviewC Moss, J BurnJournal of Medical Genetics|May 1, 1991
Sweat testing to identify female carriers of X linked hypohidrotic ectodermal dysplasiaA Clarke, J BurnDevelopmental Medicine and Child Neurology|October 1, 1991
Severe microcephaly associated with congenital varicella infectionI E Scheffer, M Baraitser, E M BrettClinical Dysmorphology|January 1, 1994
Femoral hypoplasia unusual facies syndrome with preaxial polydactylyM Baraitser, W Reardon, C Oley, et al.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 WinterPageof 60