Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Pilar Carvallo de Sq"'
Autor:
Francisca León G, Francisco López-Köstner, Gonzalo Soto D, Marjorie De la Fuente L, Demian Fullerton M, Felipe Bellolio R, Pilar Carvallo de Sq, Karin Alvarez
Publikováno v:
Revista médica de Chile v.134 n.7 2006
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Background: Among colorectal cancer hereditary variants, two syndromes show a predisposition to the disease based on germline mutations: Familial Adenomatous Polyposis (FAP) and Hereditary Nonpolyposis Colorectal Cancer (HNPCC). Aim: To screen mutati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::435c650da24675dbf14d3f0467533080
https://doi.org/10.4067/s0034-98872006000700006
https://doi.org/10.4067/s0034-98872006000700006
Determinación de una mutación en el gen BRCA1 en una familia que presenta cáncer de mama hereditario
Autor:
Paola Faúndez J, Marcela Gallardo C, Adolfo Cruz, Mario Rodriguez, Pilar Carvallo de Sq, Manuel Alvarez Z
Publikováno v:
Revista médica de Chile v.132 n.2 2004
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Background: Breast cancer is the main cause of death among women between 40 and 55 years old, in whom the hereditary cases are common. Therefore, the molecular diagnosis of germ line mutations involved in breast cancer susceptibility is relevant. BRC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4429dd3b4cad2a73853d912cc19c9288
https://doi.org/10.4067/s0034-98872004000200010
https://doi.org/10.4067/s0034-98872004000200010
Autor:
Sara Navarro V, Ruth Cave C, Graciela Molina F, Aída Milinarsky T, Marcel Deglin M, Mónica Cornejo De L, Pilar Carvallo de Sq, Francisco J González R
Publikováno v:
Revista médica de Chile, Volume: 130, Issue: 8, Pages: 850-858, Published: AUG 2002
Revista médica de Chile v.130 n.8 2002
SciELO Chile
CONICYT Chile
instacron:CONICYT
Revista médica de Chile v.130 n.8 2002
SciELO Chile
CONICYT Chile
instacron:CONICYT
Background: Cystic fibrosis (CF) is the most common autosomal recessive disease in Caucasian population. More than 900 mutations have been detected in the Cystic Fibrosis Transmembrane Regulator (CFTR) gene. The most common worldwide, is a deletion o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99bb9a8b764eebada98da14d833a4177
https://doi.org/10.4067/s0034-98872002000800002
https://doi.org/10.4067/s0034-98872002000800002
Autor:
Pilar Carvallo de Sq, Teresa Salazar C., Marcela Espinoza F, Germán Iñiguez, Fernando Cassorla G, M. Verónica Mericq
Publikováno v:
Revista médica de Chile. 129
Circulating concentrations of the high affinity growth hormone binding protein (GHBP) may be a marker of GH receptor density as well as GH sensiffvity. Goal: To determine values of GHBP for a normal Chilean pediatric population. Methods: We determine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6051bd18e25eabf1cfbfa5b3b4a6ea11
https://doi.org/10.4067/s0034-98872001000400006
https://doi.org/10.4067/s0034-98872001000400006