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Journal of Medical Genetics|September 1, 1992
Weyers' ulnar ray/oligodactyly syndrome and the association of midline malformations with ulnar ray defectsP D Turnpenny, J C Dean, P Duffty, et al.Journal of Medical Genetics|May 15, 2003
Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosisP D Turnpenny, N Whittock, J Duncan, et al.Clinical Dysmorphology|January 1, 1993
Severe prenatal infantile cortical hyperostosis (Caffey's disease)P D Turnpenny, R Davidson, E J Stockdale, et al.Clinical Dysmorphology|October 1, 1995
A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?P D Turnpenny, D C De Silva, D W Gregory, et al.Journal of Medical Genetics|April 16, 2002
Long term health and neurodevelopment in children exposed to antiepileptic drugs before birthJ C S Dean, H Hailey, S J Moore, et al.Clinical Dysmorphology|April 1, 1992
Ectrodactyly-mandibulo-facial dysostosis: case report and delineation of an entityP D Turnpenny, A W Johnston, J C Dean, et al.American Journal of Human Genetics|June 12, 1999
A gene for autosomal recessive spondylocostal dysostosis maps to 19q13.1-q13.3P D Turnpenny, M P Bulman, T M Frayling, et al.Clinical Genetics|June 18, 2004
Pseudodominant inheritance of spondylocostal dysostosis type 1 caused by two familial delta-like 3 mutationsN V Whittock, S Ellard, J Duncan, et al.Prenatal Diagnosis|October 1, 1990
Oligohydramnios sequence in a live-born infant following chorionic villus samplingP D Turnpenny, M M Hakim, R J Thwaites, et al.Developmental Medicine and Child Neurology|August 20, 2005
Characteristics of fetal anticonvulsant syndrome associated autistic disorderA D Rasalam, H Hailey, J H G Williams, et al.Pageof 3