Introduction: the Cytogenetic Prenatal Diagnosis using amniotic liquid cells contitutes the main resource in Cuba to carry out cromosomal studies in pregnant women with risk of having an afected baby. Objective: to describe main chromosomal disorders detected in the cytogenetic prenatal diagnosis in Pinar del Río Province from January 2007 to December 2012. Material and method: a descriptive, retrospective study was carried out of 2,777 patients referred to the Province Center of Medical Genetics for prenatal studies. Compiled data were: referral causes, number and types of detected chromosomal disorders, and pregnant women with a prenatal diagnosis of congenital malformations, who decided for complete gestation. Results: during that period...
El diagnóstico citogenético en líquido amniótico obtenido por amniocentesis precoz (AP) es una alter...
Artículo científico -- Universidad de Costa Rica, Instituto de Investigaciones en Salud. 1985El diag...
PURPOSE: to evaluate the outcome of fetuses with risk of chromosomal anomalies over 1:300, based on ...
Introduction: Chromosomal abnormalities are changes that affect the number and structure of chromoso...
Introduction: chromosomal abnormalities are changes that affect the number and structure of the chro...
Introduction: the creation of centers to the development of community genetics all over the municipa...
Amniotic fluid was collected from 31 high risk pregnancy women in order to conduct prenatal diagnosi...
OBJECTIVE: The development of laboratorial techniques for the prenatal diagnosis of genetic diseases...
Introduction: the cytogenetic study of peripheral blood lymphocytes is a diagnosis means much demand...
Cytogenetic diagnosis in amniotic fluid after early amniocentesis is an alternative to woman in the ...
OBJECTIVE The measurement of Nuchal translucency (NT) between 11 and 14 weeks’ gestation is a reli...
A 26-year-old mixed-race pregnant woman with a history of apparent health evaluated in a community g...
Artículo científico -- Universidad de Costa Rica, Instituto de Investigaciones en Salud. 1985Prenata...
A 26-year-old mixed-race pregnant woman with a history of apparent health evaluated in a community g...
Artículo científico -- Universidad de Costa Rica, Instituto de Investigaciones en Salud. 2003Este es...
El diagnóstico citogenético en líquido amniótico obtenido por amniocentesis precoz (AP) es una alter...
Artículo científico -- Universidad de Costa Rica, Instituto de Investigaciones en Salud. 1985El diag...
PURPOSE: to evaluate the outcome of fetuses with risk of chromosomal anomalies over 1:300, based on ...
Introduction: Chromosomal abnormalities are changes that affect the number and structure of chromoso...
Introduction: chromosomal abnormalities are changes that affect the number and structure of the chro...
Introduction: the creation of centers to the development of community genetics all over the municipa...
Amniotic fluid was collected from 31 high risk pregnancy women in order to conduct prenatal diagnosi...
OBJECTIVE: The development of laboratorial techniques for the prenatal diagnosis of genetic diseases...
Introduction: the cytogenetic study of peripheral blood lymphocytes is a diagnosis means much demand...
Cytogenetic diagnosis in amniotic fluid after early amniocentesis is an alternative to woman in the ...
OBJECTIVE The measurement of Nuchal translucency (NT) between 11 and 14 weeks’ gestation is a reli...
A 26-year-old mixed-race pregnant woman with a history of apparent health evaluated in a community g...
Artículo científico -- Universidad de Costa Rica, Instituto de Investigaciones en Salud. 1985Prenata...
A 26-year-old mixed-race pregnant woman with a history of apparent health evaluated in a community g...
Artículo científico -- Universidad de Costa Rica, Instituto de Investigaciones en Salud. 2003Este es...
El diagnóstico citogenético en líquido amniótico obtenido por amniocentesis precoz (AP) es una alter...
Artículo científico -- Universidad de Costa Rica, Instituto de Investigaciones en Salud. 1985El diag...
PURPOSE: to evaluate the outcome of fetuses with risk of chromosomal anomalies over 1:300, based on ...