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Atencion Primaria
|
March 31, 1993
[The evaluation of a diabetes program in primary care]
J I Torrente Garrido, R Delgado Canencia, E Pejenaute Labari, et al.
American Journal of Medical Genetics
|
October 23, 1997
Two new missense mutations (A105T and C110G) in the norrin gene in two Italian families with Norrie disease and familial exudative vitreoretinopathy
I Torrente, M Mangino, M Gennarelli, et al.
American Journal of Human Genetics
|
July 27, 1999
Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22
M Mangino, O Sanchez, I Torrente, et al.
Clinical Genetics
|
October 14, 2004
Identification of five novel BOR mutations in human EYA1 gene associated with branchio-oto-renal syndrome by a DHPLC-based assay
V Migliosi, E Flex, V Guida, et al.
Prenatal Diagnosis
|
June 11, 1998
First-trimester prenatal diagnosis of Ellis-van Creveld syndrome using linked microsatellite markers
I Torrente, M Mangino, A De Luca, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics
|
February 9, 1999
Tumour necrosis factor beta gene polymorphisms in myasthenia gravis
G Zelano, M M Lino, A Evoli, et al.
Neurogenetics
|
May 17, 2001
Dopamine D4 receptor (DRD4) polymorphism and adaptability trait during infancy: a longitudinal study in 1- to 5-month-old neonates
A De Luca, M Rizzardi, I Torrente, et al.
Revista Espanola De Quimioterapia : Publicacion Oficial De La Sociedad Espanola De Quimioterapia
|
February 1, 2021
[Clinical and pharmacological data in COVID-19 hospitalized nonagenarian patients]
S Ortonobes Roig, N Soler-Blanco, I Torrente Jiménez, et al.
Fetal Diagnosis and Therapy
|
October 22, 2009
Prenatal diagnosis of androgen insensitivity syndrome
S Bianca, A Cataliotti, G Bartoloni, et al.
Journal of Endocrinological Investigation
|
May 8, 2004
Evaluation of a DHPLC-based assay for rapid detection of RET germline mutations in Italian patients with medullary thyroid carcinoma
I Torrente, F Arturi, L D'Aloiso, et al.
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of 3
Search research articles
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Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
Atencion Primaria
|
March 31, 1993
[The evaluation of a diabetes program in primary care]
J I Torrente Garrido, R Delgado Canencia, E Pejenaute Labari, et al.
American Journal of Medical Genetics
|
October 23, 1997
Two new missense mutations (A105T and C110G) in the norrin gene in two Italian families with Norrie disease and familial exudative vitreoretinopathy
I Torrente, M Mangino, M Gennarelli, et al.
American Journal of Human Genetics
|
July 27, 1999
Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22
M Mangino, O Sanchez, I Torrente, et al.
Clinical Genetics
|
October 14, 2004
Identification of five novel BOR mutations in human EYA1 gene associated with branchio-oto-renal syndrome by a DHPLC-based assay
V Migliosi, E Flex, V Guida, et al.
Prenatal Diagnosis
|
June 11, 1998
First-trimester prenatal diagnosis of Ellis-van Creveld syndrome using linked microsatellite markers
I Torrente, M Mangino, A De Luca, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics
|
February 9, 1999
Tumour necrosis factor beta gene polymorphisms in myasthenia gravis
G Zelano, M M Lino, A Evoli, et al.
Neurogenetics
|
May 17, 2001
Dopamine D4 receptor (DRD4) polymorphism and adaptability trait during infancy: a longitudinal study in 1- to 5-month-old neonates
A De Luca, M Rizzardi, I Torrente, et al.
Revista Espanola De Quimioterapia : Publicacion Oficial De La Sociedad Espanola De Quimioterapia
|
February 1, 2021
[Clinical and pharmacological data in COVID-19 hospitalized nonagenarian patients]
S Ortonobes Roig, N Soler-Blanco, I Torrente Jiménez, et al.
Fetal Diagnosis and Therapy
|
October 22, 2009
Prenatal diagnosis of androgen insensitivity syndrome
S Bianca, A Cataliotti, G Bartoloni, et al.
Journal of Endocrinological Investigation
|
May 8, 2004
Evaluation of a DHPLC-based assay for rapid detection of RET germline mutations in Italian patients with medullary thyroid carcinoma
I Torrente, F Arturi, L D'Aloiso, et al.
Page
of 3