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Kavita S Reddy

Showing results (1-10 of 19) with videos related to

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Cancer Genetics and Cytogenetics|February 26, 2008
Two cases assessed for myeloid disorders had an unexpected twistKavita S Reddy
Cancer Genetics and Cytogenetics|July 12, 2008
Assessment of 1p/19q deletions by fluorescence in situ hybridization in gliomasKavita S Reddy
American Journal of Medical Genetics. Part A|September 13, 2011
An addendum to the review of jumping translocation by ReddyKavita S Reddy
American Journal of Medical Genetics. Part A|October 28, 2010
The conundrum of a jumping translocation (JT) in CVS from twins and review of JTsKavita S Reddy
BMC Medical Genetics|January 19, 2005
Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum DisorderKavita S Reddy
Cancer Genetics and Cytogenetics|May 14, 2008
Contemplations on preclinical validation of fluorescence in situ hybridization probe assay for paraffin-embedded tissues in hematologic disordersKavita S Reddy, Joseph Tripodi
Prenatal Diagnosis|January 21, 2003
Trisomy 5p in a prenatal case with ultrasound abnormalitiesKavita S Reddy, Maya Thangavelu
American Journal of Medical Genetics. Part A|February 25, 2003
Submicroscopic terminal deletion of 1p36.3 and Xp23 hidden in complex chromosome rearrangements: independent mechanism of telomere restitution on the two chromatidsKavita S Reddy, Xiaojing Yang
Prenatal Diagnosis|January 21, 2003
Prenatal management of mosaic tetrasomy 5pKavita S Reddy, Bing Huang
Leukemia & Lymphoma|June 30, 2009
A fertile XY/XX chimeric male with chronic myeloid leukemia in a minor 46,XX cell line and a history of polycythemia vera and trisomy 9 in the major 46,XY cell lineKavita S Reddy, Gary Edward Schwartz, Mehdi Jamedhor
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Cancer Genetics and Cytogenetics|February 26, 2008
Two cases assessed for myeloid disorders had an unexpected twistKavita S Reddy
Cancer Genetics and Cytogenetics|July 12, 2008
Assessment of 1p/19q deletions by fluorescence in situ hybridization in gliomasKavita S Reddy
American Journal of Medical Genetics. Part A|September 13, 2011
An addendum to the review of jumping translocation by ReddyKavita S Reddy
American Journal of Medical Genetics. Part A|October 28, 2010
The conundrum of a jumping translocation (JT) in CVS from twins and review of JTsKavita S Reddy
BMC Medical Genetics|January 19, 2005
Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum DisorderKavita S Reddy
Cancer Genetics and Cytogenetics|May 14, 2008
Contemplations on preclinical validation of fluorescence in situ hybridization probe assay for paraffin-embedded tissues in hematologic disordersKavita S Reddy, Joseph Tripodi
Prenatal Diagnosis|January 21, 2003
Trisomy 5p in a prenatal case with ultrasound abnormalitiesKavita S Reddy, Maya Thangavelu
American Journal of Medical Genetics. Part A|February 25, 2003
Submicroscopic terminal deletion of 1p36.3 and Xp23 hidden in complex chromosome rearrangements: independent mechanism of telomere restitution on the two chromatidsKavita S Reddy, Xiaojing Yang
Prenatal Diagnosis|January 21, 2003
Prenatal management of mosaic tetrasomy 5pKavita S Reddy, Bing Huang
Leukemia & Lymphoma|June 30, 2009
A fertile XY/XX chimeric male with chronic myeloid leukemia in a minor 46,XX cell line and a history of polycythemia vera and trisomy 9 in the major 46,XY cell lineKavita S Reddy, Gary Edward Schwartz, Mehdi Jamedhor
Pageof 2