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A Radha Rama Devi

Showing results (1-10 of 11) with videos related to

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European Journal of Medical Genetics|August 6, 2017
Novel mutations in SERAC1 gene in two Indian patients presenting with dystonia and intellectual disabilityA Radha Rama Devi, Lokesh Lingappa
Indian Journal of Pediatrics|April 1, 2004
Newborn screening in IndiaA Radha Rama Devi, S M Naushad
Indian Journal of Pediatrics|February 20, 2018
Challenges and Opportunities in Establishing and Maintaining Newborn Screening in a Rural Area of Andhra Pradesh - Task Force Study by Indian Council of Medical ResearchA Radha Rama Devi, Y Ananthalakshmi, K Srimannarayana Rao
Human Heredity|January 1, 1982
Inbreeding in the state of Karnataka, South IndiaA Radha Rama Devi, N A Rao, A H Bittles
Indian Journal of Pediatrics|July 4, 2006
Evaluation of total plasma homocysteine in Indian newborns using heel-prick samplesA Radha Rama Devi, S M Naushad, Krishna C Prasad
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 9, 2007
Hyperhomocysteinemia and the compound heterozygous state for methylene tetrahydrofolate reductase are independent risk factors for deep vein thrombosis among South IndiansSm Naushad, Nurul Jain Jamal, R Angalena, et al.
Brain & Development|June 14, 2015
Spectrum of mutations in Glutaryl-CoA dehydrogenase gene in glutaric aciduria type I--Study from South IndiaA Radha Rama Devi, Vakkalagadda A Ramesh, H A Nagarajaram, et al.
Journal of Cellular Biochemistry|May 18, 2012
Molecular genetic analysis of MSUD from India reveals mutations causing altered protein truncation affecting the C-termini of E1α and E1βMurali D Bashyam, Ajay K Chaudhary, Manjari Sinha, et al.
Molecular Genetics and Metabolism|March 2, 2010
Phenylalanine hydroxylase gene mutations in phenylketonuria patients from India: identification of novel mutations that affect PAH RNAMurali D Bashyam, Ajay K Chaudhary, E Chandrakanth Reddy, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
GALNS mutations in Indian patients with mucopolysaccharidosis IVAAbdul Mueed Bidchol, Ashwin Dalal, Hitesh Shah, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
European Journal of Medical Genetics|August 6, 2017
Novel mutations in SERAC1 gene in two Indian patients presenting with dystonia and intellectual disabilityA Radha Rama Devi, Lokesh Lingappa
Indian Journal of Pediatrics|April 1, 2004
Newborn screening in IndiaA Radha Rama Devi, S M Naushad
Indian Journal of Pediatrics|February 20, 2018
Challenges and Opportunities in Establishing and Maintaining Newborn Screening in a Rural Area of Andhra Pradesh - Task Force Study by Indian Council of Medical ResearchA Radha Rama Devi, Y Ananthalakshmi, K Srimannarayana Rao
Human Heredity|January 1, 1982
Inbreeding in the state of Karnataka, South IndiaA Radha Rama Devi, N A Rao, A H Bittles
Indian Journal of Pediatrics|July 4, 2006
Evaluation of total plasma homocysteine in Indian newborns using heel-prick samplesA Radha Rama Devi, S M Naushad, Krishna C Prasad
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 9, 2007
Hyperhomocysteinemia and the compound heterozygous state for methylene tetrahydrofolate reductase are independent risk factors for deep vein thrombosis among South IndiansSm Naushad, Nurul Jain Jamal, R Angalena, et al.
Brain & Development|June 14, 2015
Spectrum of mutations in Glutaryl-CoA dehydrogenase gene in glutaric aciduria type I--Study from South IndiaA Radha Rama Devi, Vakkalagadda A Ramesh, H A Nagarajaram, et al.
Journal of Cellular Biochemistry|May 18, 2012
Molecular genetic analysis of MSUD from India reveals mutations causing altered protein truncation affecting the C-termini of E1α and E1βMurali D Bashyam, Ajay K Chaudhary, Manjari Sinha, et al.
Molecular Genetics and Metabolism|March 2, 2010
Phenylalanine hydroxylase gene mutations in phenylketonuria patients from India: identification of novel mutations that affect PAH RNAMurali D Bashyam, Ajay K Chaudhary, E Chandrakanth Reddy, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
GALNS mutations in Indian patients with mucopolysaccharidosis IVAAbdul Mueed Bidchol, Ashwin Dalal, Hitesh Shah, et al.
Pageof 2