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American Journal of Hematology|February 1, 1986
T-cell chronic lymphocytic leukemia with a helper/inducer membrane phenotype: a distinct clinicopathologic subtype with a poor prognosisT E Witzig, R L Phyliky, C Y Li, et al.Mayo Clinic Proceedings|August 1, 1992
A genetic review of complete and partial hydatidiform moles and nonmolar triploidyN M Lindor, J A Ney, T A Gaffey, et al.American Journal of Medical Genetics|September 1, 1992
Xp22.3 microdeletion syndrome with microphthalmia, sclerocornea, linear skin defects, and congenital heart defectsN M Lindor, V V Michels, D A Hoppe, et al.Journal of Cellular Biochemistry|January 1, 1986
Amplification of RNA and DNA specific for erb B in unbalanced 1;7 chromosomal translocation associated with myelodysplastic syndromeG E Woloschak, G W Dewald, R S Bahn, et al.American Journal of Medical Genetics. Supplement|January 1, 1990
Hematologic disorders in 13 patients with acquired trisomy 21 and 13 individuals with Down syndromeG W Dewald, J L Diez-Martin, S L Steffen, et al.American Journal of Medical Genetics|June 1, 1993
Absence of chromosome fragility at 19q13.3 in patients with myotonic dystrophyS M Jalal, N M Lindor, V V Michels, et al.Blood|August 1, 1995
True T-cell chronic lymphocytic leukemia: a morphologic and immunophenotypic study of 25 casesJ D Hoyer, C W Ross, C Y Li, et al.Cancer Genetics and Cytogenetics|June 1, 1989
A cytogenetic study of 53 human gliomasR B Jenkins, D W Kimmel, C A Moertel, et al.Cancer Genetics and Cytogenetics|June 6, 1998
Detection of RB1 deletions by fluorescence in situ hybridization in malignant hematologic disordersA L Juneau, M Kaehler, E R Christensen, et al.Cancer Genetics and Cytogenetics|February 14, 1998
A novel three-color, clone-specific fluorescence in situ hybridization procedure for monoclonal gammopathiesG J Ahmann, S M Jalal, A L Juneau, et al.Pageof 12