Showing results (221-230 of 230) with videos related to
Sort By:
Pageof 23
You have reached the last page of results.This site can display upto 230 results.
American Journal of Medical Genetics|April 6, 1999
Acromelic frontonasal dysostosisS F Slaney, F R Goodman, B L Eilers-Walsman, et al.European Journal of Medical Genetics|July 11, 2006
European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations (ECARUCA); an online database for rare chromosome abnormalitiesI Feenstra, J Fang, D A Koolen, et al.Journal of Medical Genetics|August 1, 1997
Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosisW Reardon, D Wilkes, P Rutland, et al.Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997
Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tractF R Goodman, S Mundlos, Y Muragaki, et al.American Journal of Medical Genetics. Part A|August 25, 2004
Congenital glaucoma and brain stem atrophy as features of Aicardi-Goutières syndromeYanick J Crow, R F Massey, J R Innes, et al.Journal of Medical Genetics|January 14, 2000
Evidence for digenic inheritance in some cases of Antley-Bixler syndrome?W Reardon, A Smith, J W Honour, et al.Human Genetics|January 26, 2002
Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndromeD Kelberman, J Tyson, D C Chandler, et al.Journal of Medical Genetics|March 10, 2001
Clinical studies on submicroscopic subtelomeric rearrangements: a checklistB B de Vries, S M White, S J Knight, et al.Journal of Medical Genetics|November 14, 1997
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative studyA K Ryan, J A Goodship, D I Wilson, et al.American Journal of Human Genetics|April 6, 2000
Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome geneD M Hagan, A J Ross, T Strachan, et al.Pageof 23