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Forabosco

Showing results (211-220 of 243) with videos related to

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Nature Genetics|March 1, 1996
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndromeG Pilia, R M Hughes-Benzie, A MacKenzie, et al.
Molecular Neurodegeneration|February 26, 2016
Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysisRaffaele Ferrari, Paola Forabosco, Jana Vandrovcova, et al.
Human Mutation|January 1, 1992
Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosisM R Almeida, A Ferlini, A Forabosco, et al.
BMC Developmental Biology|July 3, 2015
FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in miceMara Marongiu, Loredana Marcia, Emanuele Pelosi, et al.
Journal of Immunogenetics|October 1, 1981
Serum immunoglobulins and lymphocyte subpopulations derangement in Turner's syndromeE Cacciari, M Masi, M P Fantini, et al.
American Journal of Human Genetics|September 14, 2002
A new essential hypertension susceptibility locus on chromosome 2p24-p25, detected by genomewide searchAndrea Angius, Enrico Petretto, Giovanni Battista Maestrale, et al.
American Journal of Medical Genetics. Part A|December 25, 2015
Duplications upstream and downstream of SHOX identified as novel causes of Leri-Weill dyschondrosteosis or idiopathic short statureDavid J Bunyan, Maria Baffico, Lucia Capone, et al.
Neurobiology of Disease|December 29, 2015
Gene co-expression networks shed light into diseases of brain iron accumulationConceição Bettencourt, Paola Forabosco, Sarah Wiethoff, et al.
Human Heredity|July 23, 2009
Meta-analysis of genome-wide linkage studies in celiac diseasePaola Forabosco, Susan L Neuhausen, Luigi Greco, et al.
Epilepsy Research|February 28, 2007
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsyElvira V De Marco, Antonio Gambardella, Ferdinanda Annesi, et al.
Pageof 25

Showing results (211-220 of 243) with videos related to

Sort By:
Pageof 25
Nature Genetics|March 1, 1996
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndromeG Pilia, R M Hughes-Benzie, A MacKenzie, et al.
Molecular Neurodegeneration|February 26, 2016
Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysisRaffaele Ferrari, Paola Forabosco, Jana Vandrovcova, et al.
Human Mutation|January 1, 1992
Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosisM R Almeida, A Ferlini, A Forabosco, et al.
BMC Developmental Biology|July 3, 2015
FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in miceMara Marongiu, Loredana Marcia, Emanuele Pelosi, et al.
Journal of Immunogenetics|October 1, 1981
Serum immunoglobulins and lymphocyte subpopulations derangement in Turner's syndromeE Cacciari, M Masi, M P Fantini, et al.
American Journal of Human Genetics|September 14, 2002
A new essential hypertension susceptibility locus on chromosome 2p24-p25, detected by genomewide searchAndrea Angius, Enrico Petretto, Giovanni Battista Maestrale, et al.
American Journal of Medical Genetics. Part A|December 25, 2015
Duplications upstream and downstream of SHOX identified as novel causes of Leri-Weill dyschondrosteosis or idiopathic short statureDavid J Bunyan, Maria Baffico, Lucia Capone, et al.
Neurobiology of Disease|December 29, 2015
Gene co-expression networks shed light into diseases of brain iron accumulationConceição Bettencourt, Paola Forabosco, Sarah Wiethoff, et al.
Human Heredity|July 23, 2009
Meta-analysis of genome-wide linkage studies in celiac diseasePaola Forabosco, Susan L Neuhausen, Luigi Greco, et al.
Epilepsy Research|February 28, 2007
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsyElvira V De Marco, Antonio Gambardella, Ferdinanda Annesi, et al.
Pageof 25