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R S Verma

Showing results (41-50 of 343) with videos related to

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Canadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie|October 1, 1986
Characterization of human chromosomal constitutive heterochromatinA Babu, R S Verma
American Journal of Hematology|January 1, 1977
The value of reverse banding in detecting bone marrow chromosomal abnormalities: translocation between chromosomes 1, 9, and 22 in a case of chronic myelogenous leukemia (CML)R S Verma, H Dosik
American Journal of Human Genetics|January 1, 1979
Precise identification of human chromosomal abnormalitiesR S Verma, H Dosik
Annals of Ophthalmology|November 1, 1985
Oncogenesis of retinoblastomaR S Verma, N Kopelowitz
Cytogenetics and Cell Genetics|January 1, 1986
Heteromorphic variants of human chromosome 4A Babu, R S Verma
Clinical Genetics|May 1, 1979
The technical variables associated with the frequencies of QFQ, RFA and CBG heteromorphisms of human chromosomesR S Verma, H Dosik
Clinical Genetics|December 1, 1987
18ph+ is a so-called normal chromosomal variantR S Verma, A Babu
Indian Journal of Experimental Biology|August 2, 2001
Chlorpyrifos induced alterations in levels of thiobarbituric acid reactive substances and glutathione in rat brainR S Verma, N Srivastava
American Journal of Obstetrics and Gynecology|November 1, 1990
Cytogenetic uncertainties surrounding the fragile X in Martin-Bell syndromeV Sindwani, R S Verma
Cytogenetics and Cell Genetics|January 1, 1979
A case of chronic myelogenous leukemia (CML) with a translocation between chromosomes 12 and 22, t(12;22)(p13;q13), resulting in a Philadelphia (Ph1) chromosomeR S Verma, H Dosik
Pageof 35

Showing results (41-50 of 343) with videos related to

Sort By:
Pageof 35
Canadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie|October 1, 1986
Characterization of human chromosomal constitutive heterochromatinA Babu, R S Verma
American Journal of Hematology|January 1, 1977
The value of reverse banding in detecting bone marrow chromosomal abnormalities: translocation between chromosomes 1, 9, and 22 in a case of chronic myelogenous leukemia (CML)R S Verma, H Dosik
American Journal of Human Genetics|January 1, 1979
Precise identification of human chromosomal abnormalitiesR S Verma, H Dosik
Annals of Ophthalmology|November 1, 1985
Oncogenesis of retinoblastomaR S Verma, N Kopelowitz
Cytogenetics and Cell Genetics|January 1, 1986
Heteromorphic variants of human chromosome 4A Babu, R S Verma
Clinical Genetics|May 1, 1979
The technical variables associated with the frequencies of QFQ, RFA and CBG heteromorphisms of human chromosomesR S Verma, H Dosik
Clinical Genetics|December 1, 1987
18ph+ is a so-called normal chromosomal variantR S Verma, A Babu
Indian Journal of Experimental Biology|August 2, 2001
Chlorpyrifos induced alterations in levels of thiobarbituric acid reactive substances and glutathione in rat brainR S Verma, N Srivastava
American Journal of Obstetrics and Gynecology|November 1, 1990
Cytogenetic uncertainties surrounding the fragile X in Martin-Bell syndromeV Sindwani, R S Verma
Cytogenetics and Cell Genetics|January 1, 1979
A case of chronic myelogenous leukemia (CML) with a translocation between chromosomes 12 and 22, t(12;22)(p13;q13), resulting in a Philadelphia (Ph1) chromosomeR S Verma, H Dosik
Pageof 35