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P Gasparini

Showing results (131-140 of 204) with videos related to

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Haematologica|May 9, 2000
Geographic distribution of CDA-II: did a founder effect operate in Southern Italy?A Iolascon, V Servedio, R Carbone, et al.
Human Mutation|July 12, 2002
Erratum: Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairmentN López-Bigas, S Melchionda, R de Cid, et al.
American Journal of Human Genetics|October 1, 1995
Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneityP Gasparini, M J Calonge, L Bisceglia, et al.
Blood|February 1, 1992
BCR breakpoint subregions and blast crisis lineage in CML patientsG Martinelli, A Chiamenti, P Gasparini, et al.
Lancet (London, England)|December 9, 1989
Delta F508 gene deletion in cystic fibrosis in southern EuropeX Estivill, M Chillon, T Casals, et al.
British Journal of Haematology|May 1, 1987
A benign form of thalassaemia intermedia may be determined by the interaction of triplicated alpha locus and heterozygous beta-thalassaemiaC Camaschella, M T Bertero, A Serra, et al.
Genomics|October 15, 1996
Genomic structure and organization of the human rBAT gene (SLC3A1)J Purroy, L Bisceglia, M J Calonge, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1990
Regional distribution of cystic fibrosis linked DNA haplotypes in Italy, a collaborative studyP Gasparini, N Cappello, B Dallapiccola, et al.
Human Genetics|September 1, 1989
Linkage disequilibrium for DNA haplotypes near the cystic fibrosis locus in two south European populationsX Estivill, P Gasparini, G Novelli, et al.
Human Genetics|April 1, 1995
New polymorphisms and markers in the HLA class I region: relevance to hereditary hemochromatosis (HFE)A Totaro, A Grifa, A Roetto, et al.
Pageof 21

Showing results (131-140 of 204) with videos related to

Sort By:
Pageof 21
Haematologica|May 9, 2000
Geographic distribution of CDA-II: did a founder effect operate in Southern Italy?A Iolascon, V Servedio, R Carbone, et al.
Human Mutation|July 12, 2002
Erratum: Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairmentN López-Bigas, S Melchionda, R de Cid, et al.
American Journal of Human Genetics|October 1, 1995
Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneityP Gasparini, M J Calonge, L Bisceglia, et al.
Blood|February 1, 1992
BCR breakpoint subregions and blast crisis lineage in CML patientsG Martinelli, A Chiamenti, P Gasparini, et al.
Lancet (London, England)|December 9, 1989
Delta F508 gene deletion in cystic fibrosis in southern EuropeX Estivill, M Chillon, T Casals, et al.
British Journal of Haematology|May 1, 1987
A benign form of thalassaemia intermedia may be determined by the interaction of triplicated alpha locus and heterozygous beta-thalassaemiaC Camaschella, M T Bertero, A Serra, et al.
Genomics|October 15, 1996
Genomic structure and organization of the human rBAT gene (SLC3A1)J Purroy, L Bisceglia, M J Calonge, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1990
Regional distribution of cystic fibrosis linked DNA haplotypes in Italy, a collaborative studyP Gasparini, N Cappello, B Dallapiccola, et al.
Human Genetics|September 1, 1989
Linkage disequilibrium for DNA haplotypes near the cystic fibrosis locus in two south European populationsX Estivill, P Gasparini, G Novelli, et al.
Human Genetics|April 1, 1995
New polymorphisms and markers in the HLA class I region: relevance to hereditary hemochromatosis (HFE)A Totaro, A Grifa, A Roetto, et al.
Pageof 21