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V Brancolini

Showing results (1-10 of 14) with videos related to

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Annali Dell'Istituto Superiore Di Sanita|January 1, 1996
Genetic linkage studies for the identification of cancer-related genesV Brancolini, M Devoto
American Journal of Medical Genetics|March 15, 1996
Exclusion of linkage between RET and neuronal intestinal dysplasia type BV Barone, D Weber, Y Luo, et al.
Electrophoresis|May 1, 1994
Capillary zone electrophoresis of polymerase chain reaction-amplified DNA fragments in polymer networks: the case of GATT microsatellites in cystic fibrosisC Gelfi, A Orsi, P G Righetti, et al.
Human Molecular Genetics|July 1, 1996
Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharingA Bolino, V Brancolini, F Bono, et al.
American Journal of Human Genetics|April 1, 1996
The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28A Auricchio, V Brancolini, G Casari, et al.
Human Genetics|September 1, 1995
Search for mutations in pancreatic sufficient cystic fibrosis Italian patients: detection of 90% of molecular defects and identification of three novel mutationsV Brancolini, L Cremonesi, E Belloni, et al.
Human Mutation|August 26, 1998
Five families with arginine 519-cysteine mutation in COL2A1: evidence for three distinct foundersJ F Bleasel, D Holderbaum, V Brancolini, et al.
Neurology|May 1, 1997
Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathyA Malandrini, P Carrera, G Ciacci, et al.
Revista De Neurologia|May 15, 1998
[Antiochian genealogies in which idiopathic epilepsy presents familial conglomeration. Simulations of power for the detection of genetic linkage]M Arcos-Burgos, L G Palacio, I Jiménez, et al.
Neurology|April 1, 1998
Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B)A Gambardella, A Bolino, M Muglia, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Annali Dell'Istituto Superiore Di Sanita|January 1, 1996
Genetic linkage studies for the identification of cancer-related genesV Brancolini, M Devoto
American Journal of Medical Genetics|March 15, 1996
Exclusion of linkage between RET and neuronal intestinal dysplasia type BV Barone, D Weber, Y Luo, et al.
Electrophoresis|May 1, 1994
Capillary zone electrophoresis of polymerase chain reaction-amplified DNA fragments in polymer networks: the case of GATT microsatellites in cystic fibrosisC Gelfi, A Orsi, P G Righetti, et al.
Human Molecular Genetics|July 1, 1996
Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharingA Bolino, V Brancolini, F Bono, et al.
American Journal of Human Genetics|April 1, 1996
The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28A Auricchio, V Brancolini, G Casari, et al.
Human Genetics|September 1, 1995
Search for mutations in pancreatic sufficient cystic fibrosis Italian patients: detection of 90% of molecular defects and identification of three novel mutationsV Brancolini, L Cremonesi, E Belloni, et al.
Human Mutation|August 26, 1998
Five families with arginine 519-cysteine mutation in COL2A1: evidence for three distinct foundersJ F Bleasel, D Holderbaum, V Brancolini, et al.
Neurology|May 1, 1997
Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathyA Malandrini, P Carrera, G Ciacci, et al.
Revista De Neurologia|May 15, 1998
[Antiochian genealogies in which idiopathic epilepsy presents familial conglomeration. Simulations of power for the detection of genetic linkage]M Arcos-Burgos, L G Palacio, I Jiménez, et al.
Neurology|April 1, 1998
Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B)A Gambardella, A Bolino, M Muglia, et al.
Pageof 2