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Journal of Medical Genetics|July 1, 1989
A possible human homologue for the mouse mutant disorganisationR M Winter, D DonnaiArchives of Disease in Childhood|June 1, 1987
Anorectal malformation: familial aspects and associated anomaliesG R Boocock, D DonnaiClinical Dysmorphology|July 1, 1994
Anencephaly with spinal dysraphism, cleft lip and palate and limb reduction defectsA Medeira, N Dennis, D DonnaiClinical Dysmorphology|October 26, 1999
Disorganisation: a case with popliteal pterygia and placental-skin appendagesL Korniszewski, A Skorka, D DonnaiJournal of Medical Genetics|January 1, 1996
X linked hydrocephalus and MASA syndromeS Kenwrick, M Jouet, D DonnaiAmerican Journal of Medical Genetics|November 15, 1993
Brachmann-de Lange syndrome. Delineation of the clinical phenotypeM Ireland, D Donnai, J BurnJournal of Medical Genetics|November 14, 1997
Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndromeA Slavotinek, L Gaunt, D DonnaiClinical Genetics|February 1, 1996
Neurofibromatosis/Noonan phenotype: a variable feature of type 1 neurofibromatosisA Colley, D Donnai, D G EvansJournal of Medical Genetics|February 1, 1987
Familial orofaciodigital syndrome type I presenting as adult polycystic kidney diseaseD Donnai, L Kerzin-Storrar, R HarrisProsthetics and Orthotics International|August 1, 1991
Heredity and dysmorphic syndromes in congenital limb deficienciesD G Evans, Y Thakker, D DonnaiPageof 13