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Human Genetics|January 1, 1984
New chromosomal syndrome: Miller-Dieker syndrome and monosomy 17p13R F Stratton, W B Dobyns, S D Airhart, et al.American Journal of Human Genetics|September 1, 1985
Fragile (X) expression induced by FUdR is transient and inversely related to levels of thymidylate synthase activityE S Cantú, R L Nussbaum, S D Airhart, et al.Cytogenetics and Cell Genetics|January 1, 1988
Localization of mouse phenylalanine hydroxylase locus on chromosome 10F D Ledley, S A Ledbetter, D H Ledbetter, et al.American Journal of Medical Genetics|August 1, 1985
A new family with fra(10)(q25): spontaneous expression and 100% expression with 100 microM BrdUS M Gollin, H G Bock, C T Caskey, et al.American Journal of Medical Genetics|February 1, 1991
New somatic cell hybrids for physical mapping in distal Xq and the fragile X regionS A Ledbetter, C E Schwartz, K E Davies, et al.Genomics|September 11, 1991
Isolation of a human chromosome 14-only somatic cell hybrid: analysis using Alu and LINE-based PCRA Mares, S A Ledbetter, D H Ledbetter, et al.Journal of Medical Genetics|October 23, 1998
Isolation of BAC clones spanning the Xq22.3 translocation breakpoint in a lissencephaly patient with a de novo X;2 translocationN Matsumoto, D T Pilz, J A Fantes, et al.Oncogene|March 2, 1995
Spatial organization of ABR and CRK genes on human chromosome band 17p13.3C Morris, S Benjes, L Haataja, et al.American Journal of Human Genetics|January 1, 1989
Precise localization of NF1 to 17q11.2 by balanced translocationD H Ledbetter, D C Rich, P O'Connell, et al.American Journal of Human Genetics|September 1, 1987
Localization of the human thyroxine-binding globulin gene to the long arm of the X chromosome (Xq21-22)J M Trent, I L Flink, E Morkin, et al.Pageof 33