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Proceedings of the National Academy of Sciences of the United States of America|June 1, 1975
Somatic rearrangement of chromosome 14 in human lymphocytesB K McCaw, F Hecht, D G Harnden, et al.Clinical Genetics|February 1, 1986
Population cytogenetics of autosomal fragile sitesP Petit, J P Fryns, H van den Berghe, et al.Cancer|February 1, 1992
X;6 translocation in a child with congenital acute lymphocytic leukemiaL A Carney, J S Kinney, R R Higgins, et al.Blood|June 1, 1989
Lack of involvement of the c-fms and N-myc genes by chromosomal translocation t(2;5)(p23;q35) common to malignancies with features of so-called malignant histiocytosisR Morgan, S D Smith, B K Hecht, et al.Blood|December 1, 1985
Leukemia with Down's syndrome: translocation between chromosomes 1 and 19 in acute myelomonocytic leukemia following transient congenital myeloproliferative syndromeR Morgan, F Hecht, M L Cleary, et al.Birth Defects Original Article Series|January 1, 1976
Human centromere mapping using teratoma dataJ Ott, F Hecht, D Linder, et al.Blood|March 1, 1986
Cytogenetic and immunophenotypic analysis of cell lines established from patients with T cell leukemia/lymphomaS D Smith, R Morgan, M P Link, et al.Clinical Genetics|March 1, 1986
Genetic control over fragile X chromosome expressionF Hecht, J P Fryns, R F Vlietinck, et al.Annals of Human Genetics|November 1, 1976
Estimating distances from the centromere by means of benign ovarian teratomas in manJ Ott, D Linder, B K McCaw, et al.Journal of Developmental and Behavioral Pediatrics : JDBP|January 1, 2013
Early identification of young children with hearing loss in federally qualified health centersParul Bhatia, Sandra Mintz, Barbara F Hecht, et al.Pageof 14