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BMJ (Clinical Research Ed.)|June 12, 1993
Uptake of cystic fibrosis testing in primary care: supply push or demand pull?H Bekker, M Modell, G Denniss, et al.American Journal of Medical Genetics. Part A|June 5, 2003
Terminal deletion of chromosome 5p in a patient with phenotypical features of Lujan-Fryns syndromeE Stathopulu, C Mackie Ogilvie, F A FlinterExperimental and Clinical Immunogenetics|January 1, 1985
Heterochromatic chromosome variation and reproductive failureM BobrowPhilosophical Transactions of the Royal Society of London. Series B, Biological Sciences|June 15, 1988
The prevention and avoidance of genetic disease: summing upM BobrowJournal of Medical Genetics|January 1, 1997
Clinical, cytogenetic, and molecular analysis of three families with FRAXEA J Barnicoat, Q Wang, J Turk, et al.Journal of Medical Genetics|May 1, 1993
Probable de novo 17q duplication (q11.2-->q21.1): a newly recognised chromosomal syndrome in a child with Klinefelter's syndromeA M Butt, D Mehta, J A Goodeve, et al.Human Mutation|March 27, 1999
Detection of mutations in COL4A5 in patients with Alport syndromeK E Plant, P M Green, D Vetrie, et al.Mutation Research|November 1, 1975
Sister chromatid exchanges--a sensitive assay of agents damaging human chromosomesE Solomon, M BobrowNature|November 6, 1980
Nonrandom segregation of nucleolar organizing chromosomes at mitosis?M Bobrow, J HeritagePageof 125