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Human Genetics|March 1, 1987
DNA deletions in mild and severe Becker muscular dystrophyK A Hart, S Hodgson, A Walker, et al.Lancet (London, England)|March 31, 1979
Amniotic-fluid acetylcholinesterase as a possible diagnostic test for neural-tube defects in early pregnancyA D Smith, N J Wald, H S Cuckle, et al.Genomics|December 1, 1992
Identification of region-specific yeast artificial chromosomes using pools of Alu element-mediated polymerase chain reaction probes labeled via linear amplificationC G Cole, K Patel, J Shipley, et al.Journal of Medical Genetics|March 1, 1987
The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophyS Hodgson, A Walker, C Cole, et al.Neuromuscular Disorders : NMD|January 1, 1992
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental abilityS V Hodgson, S Abbs, S Clark, et al.Clinical Genetics|April 1, 1989
Molecular deletions in the Duchenne/Becker muscular dystrophy geneK A Hart, S Abbs, M C Wapenaar, et al.Clinical Genetics|July 1, 1988
The gene for incontinentia pigmenti: failure of linkage studies using DNA probes to confirm cytogenetic localizationA Harris, S Lankester, E Haan, et al.British Journal of Cancer|August 19, 2007
The GRAIDS Trial: a cluster randomised controlled trial of computer decision support for the management of familial cancer risk in primary careJ Emery, H Morris, R Goodchild, et al.European Journal of Human Genetics : EJHG|January 1, 1994
Counselling following diagnosis of fetal abnormality: a comparison between German, Portuguese and UK geneticistsT Marteau, H Drake, M Reid, et al.Somatic Cell Genetics|March 1, 1976
Human gene mapping using an X/autosome translocationE Solomon, M Bobrow, P N Goodfellow, et al.Pageof 423