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Archives of Disease in Childhood|November 26, 1999
Towards earlier diagnosis of 22q11 deletionsE S Tobias, N Morrison, M L Whiteford, et al.Journal of Medical Genetics|December 1, 1990
Normal growth and development in a child with Baller-Gerold syndrome (craniosynostosis and radial aplasia)P Galea, J L TolmieTeratology|December 1, 1987
Atypical malformations in an infant exposed to warfarin during the first trimester of pregnancyP Ruthnum, J L TolmieJournal of Medical Genetics|July 1, 1996
Holoprosencephaly in the west of Scotland 1975-1994M L Whiteford, J L TolmieJournal of Medical Genetics|April 16, 1998
Recurrence risks in mental retardationY J Crow, J L TolmieJournal of Medical Genetics|July 17, 2008
Cerebro-oculo-facio-skeletal syndrome: three additional cases with CSB mutations, new diagnostic criteria and an approach to investigationV Laugel, C Dalloz, E S Tobias, et al.Neuropediatrics|March 6, 2004
Coats' plus: a progressive familial syndrome of bilateral Coats' disease, characteristic cerebral calcification, leukoencephalopathy, slow pre- and post-natal linear growth and defects of bone marrow and integumentY J Crow, J McMenamin, C A Haenggeli, et al.Archives of Disease in Childhood|January 1, 1996
Clinical and molecular cytogenetic (FISH) diagnosis of Williams syndromeC M Brewer, N Morrison, J L TolmieAmerican Journal of Medical Genetics|August 1, 1987
A lethal multiple pterygium syndrome with apparent X-linked recessive inheritanceJ L Tolmie, A Patrick, J R YatesJournal of Medical Genetics|November 1, 1987
Congenital anal anomalies in two families with the Opitz G syndromeJ L Tolmie, N Coutts, I K DrainerPageof 8