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European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|November 26, 1999
Overdose of tetracycline for pleurodesis leading to chemical burns of the pleuraH Chaugle, C Parchment, D J Keenan, 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.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.Archives of Disease in Childhood. Fetal and Neonatal Edition|October 22, 2005
Dysmorphic features: an important clue to the diagnosis and severity of fetal anticonvulsant syndromesU Kini, N Adab, J Vinten, et al.Neuropediatrics|April 12, 2003
Neuropsychological assessment of a group of UK patients with Cohen syndromeK E Chandler, M Moffett, J Clayton-Smith, et al.Journal of Medical Genetics|December 24, 1998
Locus heterogeneity in autosomal dominant congenital external ophthalmoplegia (CFEOM)G C Black, R Perveen, E Hatchwell, et al.American Journal of Medical Genetics|February 15, 1992
Recurrent Wiedemann-Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5)A M Norman, A P Read, J Clayton-Smith, et al.European Journal of Human Genetics : EJHG|July 11, 2013
Dysmorphology at a distance: results of a web-based diagnostic serviceS Douzgou, J Clayton-Smith, S Gardner, et al.Clinical Dysmorphology|May 18, 1999
Two brothers with varying combinations of severe developmental delay, epilepsy, microcephaly, tetralogy of Fallot and hydronephrosisA Ryan, J Burn, S Court, et al.European Journal of Medical Genetics|December 31, 2017
The TBR1-related autistic-spectrum-disorder phenotype and its clinical spectrumJ H McDermott, D D D Study, J Clayton-Smith, et al.Pageof 10