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Archives of Pathology & Laboratory Medicine|April 1, 1997
Pilot studies for proficiency testing using fluorescence in situ hybridization with chromosome-specific DNA probes: a College of American Pathologists/American College of Medical Genetics ProgramG W Dewald, A R Brothman, M G Butler, et al.Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie. Albrecht Von Graefe'S Archive for Clinical and Experimental Ophthalmology|October 1, 1979
Retinoblastoma Y79 cell line: a study of membrane structuresA L Green, E S Meek, D W White, et al.Prenatal Diagnosis|September 1, 1990
Trisomy 12 mosaicism in phenotypically normal fetuses following prenatal detectionH E Wyandt, T Maher, N L Fisher, et al.Cancer Genetics and Cytogenetics|April 1, 1984
Evolution to eosinophilic leukemia with a t(5:11) translocation in a patient with idiopathic hypereosinophilic syndromeT J Yoo, S V Orman, S R Patil, et al.Experimental Hematology|October 1, 1984
Marrow transplantation for stable-phase chronic granulocytic leukemiaJ O Armitage, L W Klassen, S R Patil, et al.American Journal of Medical Genetics|January 1, 1981
Deletions of different segments of the long arm of chromosome 4J A Mitchell, S Packman, W D Loughman, et al.Human Molecular Genetics|January 1, 1997
Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysisV C Sheffield, M E Pierpont, D Nishimura, et al.Blood|October 15, 1990
Trisomy 13: a new recurring chromosome abnormality in acute leukemiaH Döhner, D C Arthur, E D Ball, et al.American Journal of Medical Genetics|July 9, 1999
Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal developmentD L Freedenberg, L W Gane, C S Richards, et al.Nature Genetics|June 10, 1998
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25D Y Nishimura, R E Swiderski, W L Alward, et al.Pageof 7