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Journal of Medical Genetics|November 1, 1987
Fetal valproate syndrome: is there a recognisable phenotype?R M Winter, D Donnai, J Burn, et al.Prenatal Diagnosis|May 1, 1984
Prenatal diagnosis of mandibulofacial dysostosisK H Nicolaides, D Johansson, D Donnai, et al.Journal of Medical Genetics|August 1, 1991
De novo ring chromosome 3: a new case with a mild phenotypeM McKinley, A Colley, P Sinclair, et al.Clinical Dysmorphology|April 1, 1994
Ohdo-like blepharophimosis syndrome with distinctive facies, neonatal hypotonia, mental retardation and hypoplastic teethJ Clayton-Smith, M Krajewska-Walasek, A Fryer, et al.The British Journal of Ophthalmology|January 1, 1992
Is there a genetic basis for Fuchs' heterochromic uveitis? Discordance in monozygotic twinsN P Jones, A P ReadBMJ (Clinical Research Ed.)|February 3, 1990
Examination of fetuses after induced abortion for fetal abnormalityJ Clayton-Smith, P A Farndon, C McKeown, et al.American Journal of Medical Genetics|May 1, 1987
Proteus syndrome: an expanded phenotypeR D Clark, D Donnai, J Rogers, et al.Prenatal Diagnosis|May 1, 1994
Examination of fetuses after induced abortion for fetal abnormality--a follow-up studyA Medeira, A Norman, J Haslam, et al.Journal of Medical Genetics|November 1, 1991
The non-deletion alpha thalassaemia/mental retardation syndrome: further support for X linkageD Donnai, J Clayton-Smith, R J Gibbons, et al.Pageof 19