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European Journal of Human Genetics : EJHG|January 1, 1995
Molecular genetics of the human chondrodysplasias-1995W A HortonEndocrinology and Metabolism Clinics of North America|September 1, 1996
Molecular genetic basis of the human chondrodysplasiasW A HortonCurrent Opinion in Pediatrics|August 1, 1997
Fibroblast growth factor receptor 3 and the human chondrodysplasiasW A HortonPediatric Radiology|January 1, 1994
Extending the nosology of the chondrodysplasias to the cellular and molecular levelsW A HortonAmerican Journal of Medical Genetics|January 15, 1993
In vitro chondrogenesis in human chondrodysplasiasW A HortonAmerican Journal of Human Genetics|March 1, 1992
Huntington disease and the abuse of geneticsP S HarperBMJ (Clinical Research Ed.)|May 22, 1993
Research samples from families with genetic diseases: a proposed code of conductP S HarperClinical Genetics|November 7, 2017
Conversations with French medical geneticists. A personal perspective on the origins and early years of medical genetics in FranceP S HarperPhilosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 29, 1997
Genetic testing, life insurance, and adverse selectionP S HarperArchives of Disease in Childhood|July 1, 1975
Congenital myotonic dystrophy in Britain. II. Genetic basisP S HarperPageof 30