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Cancer Genetics and Cytogenetics|July 1, 1988
Regional chromosome localization of human papillomavirus integration sites near fragile sites, oncogenes, and cancer chromosome breakpointsL A Cannizzaro, M Dürst, M J Mendez, et al.Journal De Chirurgie|November 1, 1990
[Therapeutic diagram in advanced cancers of the esophagus]G Benhamou, J P Marmuse, H Johanet, et al.Cancer Genetics and Cytogenetics|January 1, 1985
The Philadelphia (Ph) chromosome in leukemia. II. Variant Ph translocations in acute lymphoblastic leukemiaA A Sandberg, R Morgan, T J Kipps, et al.Humangenetik|January 1, 1975
Exclusion gene mapping utilizing patients with chromosome imbalance: the HL-A system as a prototypeR E Magenis, K Overton, H Wyandt, et al.Cancer Genetics and Cytogenetics|July 1, 1988
New common fragile sitesF Hecht, E H Tajara, D Lockwood, et al.Human Genetics|March 12, 1976
9p trisomy identified by Giemsa-11H E Wyandt, F Hecht, R E Magenis, et al.Neurology|March 23, 2005
Increased rate of major malformations in offspring exposed to valproate during pregnancyD F Wyszynski, M Nambisan, T Surve, et al.American Journal of Medical Genetics|May 9, 2001
Prenatal diagnosis and molecular cytogenetics in a case of partial trisomy 14 and monosomy 21C Lee, D J Fowler, E Lemyre, et al.Obstetrics and Gynecology|March 1, 1984
Prenatal diagnosis of fragile (X) syndromeW A Hogge, S A Schonberg, T W Glover, et al.Blood|June 1, 1978
Clonal evolution in atypical chronic granulocytic leukemia: a non-Philadelphia translocationG C Bagby, B Kaiser-McCaw, F Hecht, et al.Pageof 26