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Pediatric Research|September 1, 1982
Higher incidence of small Y chromosome in humans with trisomy 21 (Down syndrome)R S Verma, A Huq, C Madahar, et al.Cancer Genetics and Cytogenetics|January 1, 1985
Unusual translocations involving chromosomes 12;22 and 9;12 in a case of chronic myelogenous leukemiaS Chemitiganti, R S Verma, R T Silver, et al.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.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.Cytobios|January 1, 1982
GTG banding is not sufficient for the localization of breakpoints in translocationsR S Verma, L Y Hsu, H Dosik, et al.American Journal of Medical Genetics|January 1, 1981
Duplication 3q: severe manifestations in an infant with duplication of a short segment of 3qW Rosenfeld, R S Verma, R C Jhaveri, et al.Journal of Cancer Research and Clinical Oncology|January 1, 1987
Chromosomal abnormalities in adult T-cell leukemia/lymphoma (ATL). A report of six cases with review of the literatureR S Verma, M J Macera, M Krishnamurthy, et al.Canadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie|December 1, 1986
Role of heterochromatin during preferential 9q;22q translocation in chronic myelogenous leukemiaR S Verma, J Rodriguez, A Babu, et al.Pageof 32