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M Upadhyaya

Showing results (1-10 of 159) with videos related to

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Neuromuscular Disorders : NMD|January 1, 1997
Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD)J Fisher, M Upadhyaya
Journal of Surgical Case Reports|June 25, 2014
Bilateral inflamed paratubal cystsM Upadhyaya, E Cusick
Human Genetics|October 30, 1999
Evaluation of the protein truncation test and mutation detection in the NF1 gene: mutational analysis of 15 known and 40 unknown mutationsM J Osborn, M Upadhyaya
Indian Journal of Psychiatry|September 20, 2011
A study of premenopausal psychiatric disordersM Upadhyaya, S K Chaturvedi
Human Genetics|October 1, 1993
A de novo nonsense mutation in exon 28 of the neurofibromatosis type 1 (NF1) geneM H Shen, M Upadhyaya
American Journal of Medical Genetics|April 24, 1995
Two single base polymorphisms in introns 41 and 16 of the NF1 geneM H Shen, M Upadhyaya
Human Mutation|August 14, 1999
Mutation analysis of iduronate-2-sulphatase gene in 24 patients with Hunter syndrome: characterisation of 6 novel mutations. Mutation in brief no. 249. OnlineC Hartog, A Fryer, M Upadhyaya
Prenatal Diagnosis|October 16, 1999
Prenatal diagnosis for facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, M MacDonald, D Ravine
Human Mutation|February 14, 2006
Functional splicing assay shows a pathogenic intronic mutation in neurofibromatosis type 1 (NF1) due to intronic sequence exonizationM Raponi, M Upadhyaya, D Baralle
Journal of Surgical Case Reports|June 20, 2014
Infected mesenteric ileocaecal dermoid cyst in a childM Upadhyaya, T Rogers, Ms Thyagrajan
Pageof 16

Showing results (1-10 of 159) with videos related to

Sort By:
Pageof 16
Neuromuscular Disorders : NMD|January 1, 1997
Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD)J Fisher, M Upadhyaya
Journal of Surgical Case Reports|June 25, 2014
Bilateral inflamed paratubal cystsM Upadhyaya, E Cusick
Human Genetics|October 30, 1999
Evaluation of the protein truncation test and mutation detection in the NF1 gene: mutational analysis of 15 known and 40 unknown mutationsM J Osborn, M Upadhyaya
Indian Journal of Psychiatry|September 20, 2011
A study of premenopausal psychiatric disordersM Upadhyaya, S K Chaturvedi
Human Genetics|October 1, 1993
A de novo nonsense mutation in exon 28 of the neurofibromatosis type 1 (NF1) geneM H Shen, M Upadhyaya
American Journal of Medical Genetics|April 24, 1995
Two single base polymorphisms in introns 41 and 16 of the NF1 geneM H Shen, M Upadhyaya
Human Mutation|August 14, 1999
Mutation analysis of iduronate-2-sulphatase gene in 24 patients with Hunter syndrome: characterisation of 6 novel mutations. Mutation in brief no. 249. OnlineC Hartog, A Fryer, M Upadhyaya
Prenatal Diagnosis|October 16, 1999
Prenatal diagnosis for facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, M MacDonald, D Ravine
Human Mutation|February 14, 2006
Functional splicing assay shows a pathogenic intronic mutation in neurofibromatosis type 1 (NF1) due to intronic sequence exonizationM Raponi, M Upadhyaya, D Baralle
Journal of Surgical Case Reports|June 20, 2014
Infected mesenteric ileocaecal dermoid cyst in a childM Upadhyaya, T Rogers, Ms Thyagrajan
Pageof 16