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American Journal of Human Genetics|June 1, 1986
Breakpoint localization of the marker chromosome associated with the cat eye syndromeA M Duncan, C A Hough, B N White, et al.
Nucleic Acids Research|March 25, 1981
Structural analysis of the three vitellogenin genes in Drosophila melanogasterD C Riddell, M J Higgins, B J McMillan, et al.
Heredity|May 15, 2008
Detecting recent speciation events: the case of the finless porpoise (genus Neophocaena)J Y Wang, T R Frasier, S C Yang, et al.
American Journal of Hematology|November 1, 1987
Carrier detection in the hemophiliasD P Lillicrap, B N White, J J Holden, et al.
Cancer Genetics and Cytogenetics|November 1, 1987
Evidence for unequal crossing-over as the mechanism for amplification of some homogeneously staining regionsJ J Holden, M R Hough, D L Reimer, et al.
International Journal of Cancer|December 6, 1997
CDKN2A mutation in a non-FAMMM kindred with cancers at multiple sites results in a functionally abnormal proteinS Sun, P M Pollock, L Liu, et al.
American Journal of Human Genetics|September 1, 1990
Genetic mapping of two new DNA markers in Xq26-q28 relative to the fragile-X syndrome locusR Sood, L M Mulligan, R Poon, et al.
Molecular Ecology|August 1, 1994
Genetic variation of the St. Lawrence beluga whale population assessed by DNA fingerprintingN J Patenaude, J S Quinn, P Beland, et al.
American Journal of Medical Genetics|August 9, 1996
A rapid, reliable, and inexpensive method for detection of di- and trinucleotide repeat markers and disease loci from dried blood spotsJ J Holden, M Chalifoux, M Wing, et al.
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