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American Journal of Medical Genetics|January 1, 1986
Inheritance of fragile X syndrome: an hypothesisJ M Friedman, P N Howard-PeeblesAmerican Journal of Medical Genetics|September 1, 1983
On the nature of folic-acid-sensitive fragile sites in human chromosomes: an hypothesisC L Krumdieck, P N Howard-PeeblesCytogenetics and Cell Genetics|January 1, 1983
Nucleolus organizer regions of the canine karyotypeP N Howard-Peebles, W M HowellClinical Genetics|April 1, 1981
Fragile sites in human chromosomes I. The effect of methionine on the Xq fragile siteP N Howard-Peebles, J C PryorAmerican Journal of Medical Genetics|September 1, 1992
Complementary duplication and deletion of 17 (pcen----p11.2): a family with a supernumerary chromosome comprised of an interstitially deleted segmentJ M Friedman, M J Harrod, P N Howard-PeeblesAmerican Journal of Medical Genetics|June 1, 1985
Wolf-Hirschhorn syndrome owing to 1:3 segregation of a maternal 4;21 translocationK Bauer, P N Howard-Peebles, D Keele, et al.Molecular and Cellular Biology|December 1, 1990
Partial deletion of alpha satellite DNA associated with reduced amounts of the centromere protein CENP-B in a mitotically stable human chromosome rearrangementR Wevrick, W C Earnshaw, P N Howard-Peebles, et al.American Journal of Medical Genetics|August 9, 1996
A fragile X mosaic male with a cryptic full mutation detected in epithelium but not in bloodA Maddalena, K N Yadvish, W C Spence, et al.The Journal of Heredity|May 1, 1980
Analysis of a marine fish cell line from a male sheepsheadP E Gregory, P N Howard-Peebles, R D Ellender, et al.American Journal of Medical Genetics|August 1, 1986
del(20p) with manifestations of arteriohepatic dysplasiaJ L Byrne, M J Harrod, J M Friedman, et al.Pageof 12