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P Gasparini

Showing results (121-130 of 204) with videos related to

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Genomics|May 1, 1991
The search for south European cystic fibrosis mutations: identification of two new mutations, four variants, and intronic sequencesP Gasparini, V Nunes, A Savoia, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Genetic homogeneity of lysinuric protein intoleranceT Lauteala, J Mykkänen, M P Sperandeo, et al.
Breast Cancer Research and Treatment|May 1, 1988
Distribution of Ha-RAS-1 proto-oncogene alleles in breast cancer patients and in a control populationG Saglio, C Camaschella, M Giai, et al.
Annales De Genetique|January 1, 1997
A recombination event close to HFE gene in hereditary hemochromatosisA Roetto, L Sbaiz, S Bosio, et al.
Human Mutation|December 19, 2001
Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairmentN López-Bigas, S Melchionda, R de Cid, et al.
Prenatal Diagnosis|June 1, 1990
Delta F508 gene deletion and prenatal diagnosis of cystic fibrosis in Italian and Spanish familiesG Novelli, F Sangiuolo, B Dallapiccola, et al.
Blood|April 21, 2001
New mutations inactivating transferrin receptor 2 in hemochromatosis type 3A Roetto, A Totaro, A Piperno, et al.
Gene|March 17, 2020
New age-related hearing loss candidate genes in humans: an ongoing challengeM Di Stazio, A Morgan, M Brumat, et al.
American Journal of Human Genetics|May 1, 1992
A frameshift mutation (2869insG) in the second transmembrane domain of the CFTR gene: identification, regional distribution, and clinical presentationV Nunes, A Bonizzato, A Gaona, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 26, 2000
Transforming growth factor-beta1 gene polymorphism, bone turnover, and bone mass in Italian postmenopausal womenF Bertoldo, L D'Agruma, F Furlan, et al.
Pageof 21

Showing results (121-130 of 204) with videos related to

Sort By:
Pageof 21
Genomics|May 1, 1991
The search for south European cystic fibrosis mutations: identification of two new mutations, four variants, and intronic sequencesP Gasparini, V Nunes, A Savoia, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Genetic homogeneity of lysinuric protein intoleranceT Lauteala, J Mykkänen, M P Sperandeo, et al.
Breast Cancer Research and Treatment|May 1, 1988
Distribution of Ha-RAS-1 proto-oncogene alleles in breast cancer patients and in a control populationG Saglio, C Camaschella, M Giai, et al.
Annales De Genetique|January 1, 1997
A recombination event close to HFE gene in hereditary hemochromatosisA Roetto, L Sbaiz, S Bosio, et al.
Human Mutation|December 19, 2001
Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairmentN López-Bigas, S Melchionda, R de Cid, et al.
Prenatal Diagnosis|June 1, 1990
Delta F508 gene deletion and prenatal diagnosis of cystic fibrosis in Italian and Spanish familiesG Novelli, F Sangiuolo, B Dallapiccola, et al.
Blood|April 21, 2001
New mutations inactivating transferrin receptor 2 in hemochromatosis type 3A Roetto, A Totaro, A Piperno, et al.
Gene|March 17, 2020
New age-related hearing loss candidate genes in humans: an ongoing challengeM Di Stazio, A Morgan, M Brumat, et al.
American Journal of Human Genetics|May 1, 1992
A frameshift mutation (2869insG) in the second transmembrane domain of the CFTR gene: identification, regional distribution, and clinical presentationV Nunes, A Bonizzato, A Gaona, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 26, 2000
Transforming growth factor-beta1 gene polymorphism, bone turnover, and bone mass in Italian postmenopausal womenF Bertoldo, L D'Agruma, F Furlan, et al.
Pageof 21