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American Journal of Medical Genetics|January 1, 1981
Double trisomy 48,XXX,+ 18 in a newbornW Rosenfeld, R S Verma, R C Jhaveri, et al.Cancer Genetics and Cytogenetics|August 1, 1992
Trisomy 8 and 11 in refractory anemia with excess blasts in transformation (RAEB-T)W R Ramirez, C J Rosenthal, S K Gogineni, et al.Genetica|October 1, 1996
A unique genomic sequence in the Wolf-Hirschhorn syndrome [WHS] region of humans is conserved in the great apesS T Tarzami, A M Kringstein, R A Conte, et al.The Journal of Biological Chemistry|February 5, 1989
Identification of a Mg2+-dependent protease in human placenta which cleaves hydrophobic folate-binding proteins to hydrophilic formsA C Antony, R S Verma, A R Unune, et al.Genes & Genetic Systems|August 27, 1998
Comparative mapping of the cri du chat and DiGeorge syndrome regions in the great apesS T Tarazami, A M Kringstein, R A Conte, et al.American Journal of Diseases of Children (1960)|October 1, 1979
Partial trisomy of chromosome 3 (3q12 leads to qter) owing to 3q/18p translocation. A trisomy 3q syndromeD Salazar, W Rosenfeld, R S Verma, et al.Experientia|April 15, 1986
Position of the Y-chromosome at somatic metaphase in patients with chronic myelogenous leukemia (CML)R S Verma, S Thomas, M Coleman, et al.Cancer Genetics and Cytogenetics|February 1, 1987
Length polymorphisms of the human Y chromosome in patients with chronic myelogenous leukemiaR S Verma, S Thomas, M Coleman, et al.Acta Haematologica|January 1, 1992
Cytogenetic evidence for extramedullary blast crisis with t(8;13)(q11;p11) in chronic myelomonocytic leukemiaP H Rao, G Cesarman, M Coleman, et al.Journal of Medical Genetics|November 14, 1997
Characterisation of a satellited non-fluorescent Y chromosome (Y[nfqs]) by FISHR S Verma, S K Gogineni, S M Kleyman, et al.Pageof 38