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P Gasparini

Showing results (91-100 of 204) with videos related to

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Journal of Medical Genetics|January 15, 2000
Leigh syndrome transmitted by uniparental disomy of chromosome 9V Tiranti, E Lamantea, G Uziel, et al.
American Journal of Human Genetics|May 1, 1996
A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23P Amati, P Gasparini, J Zlotogora, et al.
International Journal of Audiology|November 23, 2011
GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari populationM Khalifa Alkowari, G Girotto, K Abdulhadi, et al.
Biochemical and Biophysical Research Communications|October 1, 1998
GABA (gamma-amino-butyric acid) neurotransmission: identification and fine mapping of the human GABAB receptor geneA Grifa, A Totaro, J M Rommens, et al.
American Journal of Human Genetics|November 5, 1997
Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide searchP Gasparini, E Miraglia del Giudice, J Delaunay, et al.
Metabolism: Clinical and Experimental|August 25, 1999
Hyperinsulinemia in a normal population as a predictor of non-insulin-dependent diabetes mellitus, hypertension, and coronary heart disease: the Barilla factory revisitedI Zavaroni, L Bonini, P Gasparini, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Linkage analysis in two large Italian pedigrees affected with nail patella syndromeS Melchionda, M Seri, M Carella, et al.
Oral Diseases|May 10, 2017
LTF and DEFB1 polymorphisms are associated with susceptibility toward chronic periodontitis developmentL Zupin, A Robino, C O Navarra, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Evidence of linkage between susceptibility to multiple sclerosis and HLA-class II loci in Italian multiplex familiesM Eoli, M Pandolfo, A Amoroso, et al.
Blood|April 27, 1999
Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis)A Iolascon, G W Stewart, J F Ajetunmobi, et al.
Pageof 21

Showing results (91-100 of 204) with videos related to

Sort By:
Pageof 21
Journal of Medical Genetics|January 15, 2000
Leigh syndrome transmitted by uniparental disomy of chromosome 9V Tiranti, E Lamantea, G Uziel, et al.
American Journal of Human Genetics|May 1, 1996
A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23P Amati, P Gasparini, J Zlotogora, et al.
International Journal of Audiology|November 23, 2011
GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari populationM Khalifa Alkowari, G Girotto, K Abdulhadi, et al.
Biochemical and Biophysical Research Communications|October 1, 1998
GABA (gamma-amino-butyric acid) neurotransmission: identification and fine mapping of the human GABAB receptor geneA Grifa, A Totaro, J M Rommens, et al.
American Journal of Human Genetics|November 5, 1997
Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide searchP Gasparini, E Miraglia del Giudice, J Delaunay, et al.
Metabolism: Clinical and Experimental|August 25, 1999
Hyperinsulinemia in a normal population as a predictor of non-insulin-dependent diabetes mellitus, hypertension, and coronary heart disease: the Barilla factory revisitedI Zavaroni, L Bonini, P Gasparini, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Linkage analysis in two large Italian pedigrees affected with nail patella syndromeS Melchionda, M Seri, M Carella, et al.
Oral Diseases|May 10, 2017
LTF and DEFB1 polymorphisms are associated with susceptibility toward chronic periodontitis developmentL Zupin, A Robino, C O Navarra, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Evidence of linkage between susceptibility to multiple sclerosis and HLA-class II loci in Italian multiplex familiesM Eoli, M Pandolfo, A Amoroso, et al.
Blood|April 27, 1999
Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis)A Iolascon, G W Stewart, J F Ajetunmobi, et al.
Pageof 21