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Ishwar C Verma

Showing results (11-20 of 79) with videos related to

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Laboratory Medicine|August 26, 2016
Does Formaldehyde Increase Cell Free DNA in Maternal Plasma Specimens?Rintu R Jacob, Renu Saxena, Ishwar C Verma
Clinics in Laboratory Medicine|June 26, 2012
Down syndrome in India--diagnosis, screening, and prenatal diagnosisIshwar C Verma, Meena Lall, Ratna Dua Puri
Indian Journal of Pediatrics|December 26, 2022
The Indian Journal of Pediatrics: A Journey of Nine DecadesRakesh Lodha, Sushil K Kabra, Ishwar C Verma
Atherosclerosis|November 7, 2016
Spectrum of mutations in homozygous familial hypercholesterolemia in India, with four novel mutationsNitika Setia, Renu Saxena, Anjali Arora, et al.
Journal of Pediatric Genetics|October 21, 2022
A Further Case of Larsen's Syndrome: Clinical and Genotypic Challenges in DiagnosisVeronica Arora, Swasti Pal, Samarth Kulshreshtha, et al.
Indian Journal of Human Genetics|May 30, 2013
Pharmacogenetic typing for oral anti-coagulant response among factor V Leiden mutation carriersRisha Nahar, Renu Saxena, Roumi Deb, et al.
Indian Journal of Pediatrics|December 9, 2014
Newborn screening: need of the hour in IndiaIshwar C Verma, Sunita Bijarnia-Mahay, Geetu Jhingan, et al.
Breast Care (Basel, Switzerland)|June 1, 2017
Next-Generation Sequencing Reveals a Nonsense Mutation (p.Arg364Ter) in <i>MRE11A</i> Gene in an Indian Patient with Familial Breast CancerPratibha Sharma Bhai, Deepak Sharma, Renu Saxena, et al.
Indian Journal of Pediatrics|October 27, 2017
Expanding the Phenotype of the Founder South Asian Mutation in the Nuclear Encoding Mitochondrial RMND1 GeneN Vinu, Ratna D Puri, Kanav Anand, et al.
American Journal of Medical Genetics. Part A|December 5, 2012
Do parental perceptions and motivations towards genetic testing and prenatal diagnosis for deafness vary in different cultures?Risha Nahar, Ratna D Puri, Renu Saxena, et al.
Pageof 8

Showing results (11-20 of 79) with videos related to

Sort By:
Pageof 8
Laboratory Medicine|August 26, 2016
Does Formaldehyde Increase Cell Free DNA in Maternal Plasma Specimens?Rintu R Jacob, Renu Saxena, Ishwar C Verma
Clinics in Laboratory Medicine|June 26, 2012
Down syndrome in India--diagnosis, screening, and prenatal diagnosisIshwar C Verma, Meena Lall, Ratna Dua Puri
Indian Journal of Pediatrics|December 26, 2022
The Indian Journal of Pediatrics: A Journey of Nine DecadesRakesh Lodha, Sushil K Kabra, Ishwar C Verma
Atherosclerosis|November 7, 2016
Spectrum of mutations in homozygous familial hypercholesterolemia in India, with four novel mutationsNitika Setia, Renu Saxena, Anjali Arora, et al.
Journal of Pediatric Genetics|October 21, 2022
A Further Case of Larsen's Syndrome: Clinical and Genotypic Challenges in DiagnosisVeronica Arora, Swasti Pal, Samarth Kulshreshtha, et al.
Indian Journal of Human Genetics|May 30, 2013
Pharmacogenetic typing for oral anti-coagulant response among factor V Leiden mutation carriersRisha Nahar, Renu Saxena, Roumi Deb, et al.
Indian Journal of Pediatrics|December 9, 2014
Newborn screening: need of the hour in IndiaIshwar C Verma, Sunita Bijarnia-Mahay, Geetu Jhingan, et al.
Breast Care (Basel, Switzerland)|June 1, 2017
Next-Generation Sequencing Reveals a Nonsense Mutation (p.Arg364Ter) in <i>MRE11A</i> Gene in an Indian Patient with Familial Breast CancerPratibha Sharma Bhai, Deepak Sharma, Renu Saxena, et al.
Indian Journal of Pediatrics|October 27, 2017
Expanding the Phenotype of the Founder South Asian Mutation in the Nuclear Encoding Mitochondrial RMND1 GeneN Vinu, Ratna D Puri, Kanav Anand, et al.
American Journal of Medical Genetics. Part A|December 5, 2012
Do parental perceptions and motivations towards genetic testing and prenatal diagnosis for deafness vary in different cultures?Risha Nahar, Ratna D Puri, Renu Saxena, et al.
Pageof 8