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Genomics
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May 1, 1991
The search for south European cystic fibrosis mutations: identification of two new mutations, four variants, and intronic sequences
P Gasparini, V Nunes, A Savoia, et al.
European Journal of Human Genetics : EJHG
|
January 15, 1999
Genetic homogeneity of lysinuric protein intolerance
T 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 population
G Saglio, C Camaschella, M Giai, et al.
Annales De Genetique
|
January 1, 1997
A recombination event close to HFE gene in hereditary hemochromatosis
A 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 impairment
N 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 families
G Novelli, F Sangiuolo, B Dallapiccola, et al.
Blood
|
April 21, 2001
New mutations inactivating transferrin receptor 2 in hemochromatosis type 3
A Roetto, A Totaro, A Piperno, et al.
Gene
|
March 17, 2020
New age-related hearing loss candidate genes in humans: an ongoing challenge
M 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 presentation
V 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 women
F Bertoldo, L D'Agruma, F Furlan, et al.
Page
of 21
Search research articles
Search
Showing results (121-130 of 204) with videos related to
Sort By:
Page
of 21
Genomics
|
May 1, 1991
The search for south European cystic fibrosis mutations: identification of two new mutations, four variants, and intronic sequences
P Gasparini, V Nunes, A Savoia, et al.
European Journal of Human Genetics : EJHG
|
January 15, 1999
Genetic homogeneity of lysinuric protein intolerance
T 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 population
G Saglio, C Camaschella, M Giai, et al.
Annales De Genetique
|
January 1, 1997
A recombination event close to HFE gene in hereditary hemochromatosis
A 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 impairment
N 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 families
G Novelli, F Sangiuolo, B Dallapiccola, et al.
Blood
|
April 21, 2001
New mutations inactivating transferrin receptor 2 in hemochromatosis type 3
A Roetto, A Totaro, A Piperno, et al.
Gene
|
March 17, 2020
New age-related hearing loss candidate genes in humans: an ongoing challenge
M 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 presentation
V 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 women
F Bertoldo, L D'Agruma, F Furlan, et al.
Page
of 21