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V H Sankar

Showing results (1-10 of 15) with videos related to

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Indian Pediatrics|April 6, 2006
Ring chromosome 13 in an infant with ambiguous genitaliaV H Sankar, Shubha R Phadke
Indian Journal of Pediatrics|February 24, 2010
Polydactyly and genesShubha R Phadke, V H Sankar
Journal of Perinatology : Official Journal of the California Perinatal Association|March 17, 2006
Clinical utility of fetal autopsy and comparison with prenatal ultrasound findingsV H Sankar, S R Phadke
Indian Journal of Pediatrics|January 5, 2007
Asphyxiating thoracic dystrophy with facial dysmorphismV H Sankar, Shubha R Phadke
Indian Pediatrics|June 21, 2020
An Untold Tale of Iron Deficiency AnemiaLalitha Kailas, C H Umair, V H Sankar
Clinical Genetics|July 4, 2006
Ferroportin (SLC40A1) gene in thalassemic patients of Indian descentS Agarwal, V H Sankar, D Tewari, et al.
Journal of Dermatological Science|July 23, 2016
A novel large deletion that encompasses EDA and the downstream gene AWAT2 causes X-linked hypohidrotic/anhidrotic ectodermal dysplasiaAjay K Chaudhary, V H Sankar, Murali D Bashyam
Prenatal Diagnosis|June 2, 2006
Urorectal septum malformation presenting as nonimmune hydrops fetalisPradhan Mandakini, Dalal Ashwin, R Manisha, et al.
Indian Journal of Medical Sciences|January 4, 2005
T1 and M1 polymorphism in glutathione S-transferase gene and coronary artery disease in North Indian populationK M Girisha, A Gilmour, S Mastana, et al.
Indian Journal of Medical Sciences|April 5, 2005
TNFR2 gene polymorphism in coronary artery diseaseV H Sankar, K M Girisha, A Gilmour, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Indian Pediatrics|April 6, 2006
Ring chromosome 13 in an infant with ambiguous genitaliaV H Sankar, Shubha R Phadke
Indian Journal of Pediatrics|February 24, 2010
Polydactyly and genesShubha R Phadke, V H Sankar
Journal of Perinatology : Official Journal of the California Perinatal Association|March 17, 2006
Clinical utility of fetal autopsy and comparison with prenatal ultrasound findingsV H Sankar, S R Phadke
Indian Journal of Pediatrics|January 5, 2007
Asphyxiating thoracic dystrophy with facial dysmorphismV H Sankar, Shubha R Phadke
Indian Pediatrics|June 21, 2020
An Untold Tale of Iron Deficiency AnemiaLalitha Kailas, C H Umair, V H Sankar
Clinical Genetics|July 4, 2006
Ferroportin (SLC40A1) gene in thalassemic patients of Indian descentS Agarwal, V H Sankar, D Tewari, et al.
Journal of Dermatological Science|July 23, 2016
A novel large deletion that encompasses EDA and the downstream gene AWAT2 causes X-linked hypohidrotic/anhidrotic ectodermal dysplasiaAjay K Chaudhary, V H Sankar, Murali D Bashyam
Prenatal Diagnosis|June 2, 2006
Urorectal septum malformation presenting as nonimmune hydrops fetalisPradhan Mandakini, Dalal Ashwin, R Manisha, et al.
Indian Journal of Medical Sciences|January 4, 2005
T1 and M1 polymorphism in glutathione S-transferase gene and coronary artery disease in North Indian populationK M Girisha, A Gilmour, S Mastana, et al.
Indian Journal of Medical Sciences|April 5, 2005
TNFR2 gene polymorphism in coronary artery diseaseV H Sankar, K M Girisha, A Gilmour, et al.
Pageof 2