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P Amati

Showing results (61-70 of 79) with videos related to

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The Journal of Pathology|November 5, 1999
Histology of familial thyroid tumours linked to a gene mapping to chromosome 19p13.2H R Harach, F Lesueur, P Amati, et al.
European Neurology|July 17, 2012
OPA3--related autosomal dominant optic atrophy and cataract with ataxia and areflexiaX Ayrignac, C Liauzun, G Lenaers, et al.
Surgery|December 22, 1999
Mapping of a gene predisposing to familial thyroid tumors with cell oxyphilia to chromosome 19 and exclusion of JUN B as a candidate geneJ L Kraimps, F Canzian, C Jost, et al.
Journal of Medical Genetics|December 1, 1998
Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotypeM Longy, V Coulon, B Duboué, et al.
Neurology|February 22, 2008
Multiple sclerosis-like disorder in OPA1-related autosomal dominant optic atrophyC Verny, D Loiseau, C Scherer, et al.
Cytogenetics and Cell Genetics|April 25, 2000
RET rearrangements in papillary thyroid carcinomas and adenomas detected by interphase FISHR Cinti, L Yin, K Ilc, et al.
American Journal of Human Genetics|April 1, 1996
An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3pJ A Kaukonen, P Amati, A Suomalainen, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 16, 1999
Anderson's disease: exclusion of apolipoprotein and intracellular lipid transport genesA H Dannoura, N Berriot-Varoqueaux, P Amati, et al.
Eye (London, England)|November 19, 2016
Multiethnic involvement in autosomal-dominant optic atrophy in SingaporeJ L Loo, S Singhal, A V Rukmini, et al.
Neurology|April 27, 2011
Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMTJ Cassereau, C Casasnovas, N Gueguen, et al.
Pageof 8

Showing results (61-70 of 79) with videos related to

Sort By:
Pageof 8
The Journal of Pathology|November 5, 1999
Histology of familial thyroid tumours linked to a gene mapping to chromosome 19p13.2H R Harach, F Lesueur, P Amati, et al.
European Neurology|July 17, 2012
OPA3--related autosomal dominant optic atrophy and cataract with ataxia and areflexiaX Ayrignac, C Liauzun, G Lenaers, et al.
Surgery|December 22, 1999
Mapping of a gene predisposing to familial thyroid tumors with cell oxyphilia to chromosome 19 and exclusion of JUN B as a candidate geneJ L Kraimps, F Canzian, C Jost, et al.
Journal of Medical Genetics|December 1, 1998
Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotypeM Longy, V Coulon, B Duboué, et al.
Neurology|February 22, 2008
Multiple sclerosis-like disorder in OPA1-related autosomal dominant optic atrophyC Verny, D Loiseau, C Scherer, et al.
Cytogenetics and Cell Genetics|April 25, 2000
RET rearrangements in papillary thyroid carcinomas and adenomas detected by interphase FISHR Cinti, L Yin, K Ilc, et al.
American Journal of Human Genetics|April 1, 1996
An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3pJ A Kaukonen, P Amati, A Suomalainen, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 16, 1999
Anderson's disease: exclusion of apolipoprotein and intracellular lipid transport genesA H Dannoura, N Berriot-Varoqueaux, P Amati, et al.
Eye (London, England)|November 19, 2016
Multiethnic involvement in autosomal-dominant optic atrophy in SingaporeJ L Loo, S Singhal, A V Rukmini, et al.
Neurology|April 27, 2011
Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMTJ Cassereau, C Casasnovas, N Gueguen, et al.
Pageof 8