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S Danda

Showing results (11-20 of 17) with videos related to

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Clinical and Experimental Dermatology|December 8, 2020
Co-occurrence of Aicardi-Goutières syndrome type 6 and dyschromatosis symmetrica hereditaria due to compound heterozygous pathogenic variants in ADAR1: a case series from IndiaD Sathishkumar, K Muthusamy, A Gupta, et al.
Kidney International|December 1, 2005
Kidney involvement in a nongenetic rat model of type 2 diabetesRatna S Danda, Nusrath M Habiba, Hernan Rincon-Choles, et al.
The Indian Journal of Medical Research|January 1, 1997
Genotype-phenotype correlation in Duchenne/Becker muscular dystrophy patients seen at LucknowB Mittal, V Singh, S Mishra, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 12, 2016
The novel EDAR p.L397H missense mutation causes autosomal dominant hypohidrotic ectodermal dysplasiaA K Chaudhary, R Mohapatra, H A Nagarajaram, et al.
Clinical Genetics|December 21, 2013
Molecular analyses of novel ASAH1 mutations causing Farber lipogranulomatosis: analyses of exonic splicing enhancer inactivating mutationM D Bashyam, A K Chaudhary, M Kiran, et al.
Journal of Medical Genetics|February 4, 2005
Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effectP Brouillard, M Ghassibé, A Penington, et al.
Clinical Genetics|May 6, 2016
Identification and characterization of 20 novel pathogenic variants in 60 unrelated Indian patients with mucopolysaccharidoses type I and type IIA Uttarilli, P Ranganath, D Matta, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Clinical and Experimental Dermatology|December 8, 2020
Co-occurrence of Aicardi-Goutières syndrome type 6 and dyschromatosis symmetrica hereditaria due to compound heterozygous pathogenic variants in ADAR1: a case series from IndiaD Sathishkumar, K Muthusamy, A Gupta, et al.
Kidney International|December 1, 2005
Kidney involvement in a nongenetic rat model of type 2 diabetesRatna S Danda, Nusrath M Habiba, Hernan Rincon-Choles, et al.
The Indian Journal of Medical Research|January 1, 1997
Genotype-phenotype correlation in Duchenne/Becker muscular dystrophy patients seen at LucknowB Mittal, V Singh, S Mishra, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 12, 2016
The novel EDAR p.L397H missense mutation causes autosomal dominant hypohidrotic ectodermal dysplasiaA K Chaudhary, R Mohapatra, H A Nagarajaram, et al.
Clinical Genetics|December 21, 2013
Molecular analyses of novel ASAH1 mutations causing Farber lipogranulomatosis: analyses of exonic splicing enhancer inactivating mutationM D Bashyam, A K Chaudhary, M Kiran, et al.
Journal of Medical Genetics|February 4, 2005
Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effectP Brouillard, M Ghassibé, A Penington, et al.
Clinical Genetics|May 6, 2016
Identification and characterization of 20 novel pathogenic variants in 60 unrelated Indian patients with mucopolysaccharidoses type I and type IIA Uttarilli, P Ranganath, D Matta, et al.
Pageof 2