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Zeitschrift Fur Kinderchirurgie : Organ Der Deutschen, Der Schweizerischen Und Der Osterreichischen Gesellschaft Fur Kinderchirurgie = Surgery in Infancy and Childhood|December 1, 1988
A survey of neural tube defect pregnancies in north-west EnglandS H Bernard, J P Walsworth-Bell, M Super, et al.Human Molecular Genetics|January 1, 1997
Localization of a gene for oculodentodigital syndrome to human chromosome 6q22-q24A Gladwin, D Donnai, K Metcalfe, et al.Genome Research|October 6, 1999
Duplications on human chromosome 22 reveal a novel Ret Finger Protein-like gene family with sense and endogenous antisense transcriptsE Seroussi, D Kedra, H Q Pan, et al.Human Molecular Genetics|June 1, 1992
Characterization of a YAC containing part or all of the Norrie disease locusZ Y Chen, K B Sims, M Coleman, et al.Human Mutation|December 19, 2001
A survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individualsN Elanko, J S Sibbring, K A Metcalfe, et al.Journal of Medical Genetics|December 1, 1992
A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severityD G Evans, S M Huson, D Donnai, et al.Lancet (London, England)|October 3, 1987
Clinic experience of prenatal diagnosis of cystic fibrosis by use of linked DNA probesM Super, A Ivinson, M Schwarz, et al.Advances in Oto-Rhino-Laryngology|January 25, 2007
The genetics of otosclerosis: pedigree studies and linkage analysisS R Saeed, M Briggs, C Lobo, et al.Clinical Genetics|August 1, 1994
The influence of genetic counselling in the era of DNA testing on knowledge, reproductive intentions and psychological wellbeingR J Rona, R Beech, S Mandalia, et al.Nature|February 13, 1992
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box geneM Tassabehji, A P Read, V E Newton, et al.Pageof 19