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Ishwar Chander Verma

Showing results (1-10 of 34) with videos related to

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Indian Journal of Pediatrics|February 15, 2020
Genetic Testing in Pediatric Kidney DiseaseVeronica Arora, Kanav Anand, Ishwar Chander Verma
Indian Journal of Pediatrics|October 4, 2017
Genetic Testing in Pediatric OphthalmologyIshwar Chander Verma, Preeti Paliwal, Kanika Singh
Clinical Dysmorphology|March 14, 2020
A further case of hypotonia, ataxia, developmental delay and tooth enamel defect syndrome due to a recurrent C-terminal binding protein 1 mutationSameer Kumar Bhatia, Veronica Arora, Ishwar Chander Verma
Genetic Testing and Molecular Biomarkers|June 30, 2015
Noninvasive Diagnosis of Fetal Gender: Utility of Combining DYS14 and SRYRintu Rebecca Jacob, Renu Saxena, Ishwar Chander Verma
Cancer Genetics|July 13, 2019
A novel CHEK2 variant identified by next generation sequencing in an Indian family with hereditary breast cancer syndromePratibha Bhai, Renu Saxena, Samarth Kulshrestha, et al.
Journal of Human Reproductive Sciences|February 13, 2018
Prevalence of Cytogenetic Anomalies in Couples with Recurrent Miscarriages: A Case-control StudyVishali Kalotra, Meena Lall, Pushpa Saviour, et al.
Genetic Testing and Molecular Biomarkers|January 25, 2011
Mutation studies in the CFTR gene in Asian Indian subjects with congenital bilateral absence of vas deferens: report of two novel mutations and four novel variantsKabir Sachdeva, Renu Saxena, Abha Majumdar, et al.
Genetic Testing and Molecular Biomarkers|March 8, 2011
Use of ethnicity-specific sequence tag site markers for Y chromosome microdeletion studiesKabir Sachdeva, Renu Saxena, Abha Majumdar, et al.
Annals of Indian Academy of Neurology|July 2, 2020
Case Series of Creatine Deficiency Syndrome due to Guanidinoacetate Methyltransferase DeficiencyVinu Narayan, Sunita Bijarnia Mahay, Ishwar Chander Verma, et al.
Journal of Pediatric Genetics|February 8, 2021
Complete Labyrinthine Aplasia: A Unique Sign for Targeted Genetic Testing in Hearing LossMeenakshi Lallar, Veronica Arora, Renu Saxena, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Indian Journal of Pediatrics|February 15, 2020
Genetic Testing in Pediatric Kidney DiseaseVeronica Arora, Kanav Anand, Ishwar Chander Verma
Indian Journal of Pediatrics|October 4, 2017
Genetic Testing in Pediatric OphthalmologyIshwar Chander Verma, Preeti Paliwal, Kanika Singh
Clinical Dysmorphology|March 14, 2020
A further case of hypotonia, ataxia, developmental delay and tooth enamel defect syndrome due to a recurrent C-terminal binding protein 1 mutationSameer Kumar Bhatia, Veronica Arora, Ishwar Chander Verma
Genetic Testing and Molecular Biomarkers|June 30, 2015
Noninvasive Diagnosis of Fetal Gender: Utility of Combining DYS14 and SRYRintu Rebecca Jacob, Renu Saxena, Ishwar Chander Verma
Cancer Genetics|July 13, 2019
A novel CHEK2 variant identified by next generation sequencing in an Indian family with hereditary breast cancer syndromePratibha Bhai, Renu Saxena, Samarth Kulshrestha, et al.
Journal of Human Reproductive Sciences|February 13, 2018
Prevalence of Cytogenetic Anomalies in Couples with Recurrent Miscarriages: A Case-control StudyVishali Kalotra, Meena Lall, Pushpa Saviour, et al.
Genetic Testing and Molecular Biomarkers|January 25, 2011
Mutation studies in the CFTR gene in Asian Indian subjects with congenital bilateral absence of vas deferens: report of two novel mutations and four novel variantsKabir Sachdeva, Renu Saxena, Abha Majumdar, et al.
Genetic Testing and Molecular Biomarkers|March 8, 2011
Use of ethnicity-specific sequence tag site markers for Y chromosome microdeletion studiesKabir Sachdeva, Renu Saxena, Abha Majumdar, et al.
Annals of Indian Academy of Neurology|July 2, 2020
Case Series of Creatine Deficiency Syndrome due to Guanidinoacetate Methyltransferase DeficiencyVinu Narayan, Sunita Bijarnia Mahay, Ishwar Chander Verma, et al.
Journal of Pediatric Genetics|February 8, 2021
Complete Labyrinthine Aplasia: A Unique Sign for Targeted Genetic Testing in Hearing LossMeenakshi Lallar, Veronica Arora, Renu Saxena, et al.
Pageof 4