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Pharmacological Reports : PR
|
April 9, 2013
Variability in CYP2C9 allele frequency: a pilot study of its predicted impact on warfarin response among healthy South and North Indians
Risha Nahar, Roumi Deb, Renu Saxena, et al.
Genetic Testing and Molecular Biomarkers
|
February 4, 2012
Mutation analysis of the CFTR gene in 225 children: identification of five novel severe and seven reported severe mutations
Kabir Sachdeva, Renu Saxena, Ratna Puri, et al.
Indian Journal of Pediatrics
|
July 27, 2012
Survival analysis of Down syndrome cohort in a tertiary health care center in India
Risha Nahar, Udhaya Kotecha, Ratna Dua Puri, et al.
Annals of Indian Academy of Neurology
|
August 27, 2021
<i>LMNB1</i> Duplication-Mediated Autosomal Dominant Adult-Onset Leukodystrophy in an Indian Family
Sunita Bijarnia-Mahay, Gaurav Roy, Quasar S Padiath, et al.
American Journal of Medical Genetics. Part A
|
May 21, 2016
Is the diagnostic yield influenced by the indication for fetal autopsy?
Ratna Dua Puri, Udhaya Kotecha, Meena Lall, et al.
International Journal of Molecular and Cellular Medicine
|
April 24, 2018
Vascular Endothelial Growth Factor (VEGF) Gene Promoter Polymorphisms and Disease Progression in North Indian Cohort with Autosomal Dominant Polycystic Kidney Disease
Shewata Pandita, Deepshikha Maurya, Vijaya Ramachandran, et al.
Indian Journal of Gastroenterology : Official Journal of the Indian Society of Gastroenterology
|
November 16, 2020
Spectrum of mutations in genes associated with familial colorectal cancer syndrome (MLH1, MSH2, PMS2, MSH6, and APC): A not so common hereditary cancer syndrome in Indian population
Pratibha Bhai, Samarth Kulshrestha, Ratna D Puri, et al.
The Indian Journal of Medical Research
|
September 16, 2014
Molecular evaluation of a novel missense mutation & an insertional truncating mutation in SUMF1 gene
Udhaya H Kotecha, Sireesha Movva, Deepak Sharma, et al.
Indian Journal of Pediatrics
|
May 3, 2020
Mutation Spectrum of Dystrophinopathies in India: Implications for Therapy
Sudha Kohli, Renu Saxena, Elizabeth Thomas, et al.
Birth Defects Research
|
August 29, 2018
Fetal valproate syndrome as a phenocopy of Kleefstra syndrome
Veronica Arora, Anju Joshi, Meena Lall, et al.
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Search research articles
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Showing results (11-20 of 34) with videos related to
Sort By:
Page
of 4
Pharmacological Reports : PR
|
April 9, 2013
Variability in CYP2C9 allele frequency: a pilot study of its predicted impact on warfarin response among healthy South and North Indians
Risha Nahar, Roumi Deb, Renu Saxena, et al.
Genetic Testing and Molecular Biomarkers
|
February 4, 2012
Mutation analysis of the CFTR gene in 225 children: identification of five novel severe and seven reported severe mutations
Kabir Sachdeva, Renu Saxena, Ratna Puri, et al.
Indian Journal of Pediatrics
|
July 27, 2012
Survival analysis of Down syndrome cohort in a tertiary health care center in India
Risha Nahar, Udhaya Kotecha, Ratna Dua Puri, et al.
Annals of Indian Academy of Neurology
|
August 27, 2021
<i>LMNB1</i> Duplication-Mediated Autosomal Dominant Adult-Onset Leukodystrophy in an Indian Family
Sunita Bijarnia-Mahay, Gaurav Roy, Quasar S Padiath, et al.
American Journal of Medical Genetics. Part A
|
May 21, 2016
Is the diagnostic yield influenced by the indication for fetal autopsy?
Ratna Dua Puri, Udhaya Kotecha, Meena Lall, et al.
International Journal of Molecular and Cellular Medicine
|
April 24, 2018
Vascular Endothelial Growth Factor (VEGF) Gene Promoter Polymorphisms and Disease Progression in North Indian Cohort with Autosomal Dominant Polycystic Kidney Disease
Shewata Pandita, Deepshikha Maurya, Vijaya Ramachandran, et al.
Indian Journal of Gastroenterology : Official Journal of the Indian Society of Gastroenterology
|
November 16, 2020
Spectrum of mutations in genes associated with familial colorectal cancer syndrome (MLH1, MSH2, PMS2, MSH6, and APC): A not so common hereditary cancer syndrome in Indian population
Pratibha Bhai, Samarth Kulshrestha, Ratna D Puri, et al.
The Indian Journal of Medical Research
|
September 16, 2014
Molecular evaluation of a novel missense mutation & an insertional truncating mutation in SUMF1 gene
Udhaya H Kotecha, Sireesha Movva, Deepak Sharma, et al.
Indian Journal of Pediatrics
|
May 3, 2020
Mutation Spectrum of Dystrophinopathies in India: Implications for Therapy
Sudha Kohli, Renu Saxena, Elizabeth Thomas, et al.
Birth Defects Research
|
August 29, 2018
Fetal valproate syndrome as a phenocopy of Kleefstra syndrome
Veronica Arora, Anju Joshi, Meena Lall, et al.
Page
of 4