Background: Fetal sex determination is useful for families at risk of X-linked disorders, such as Duchenne muscular dystrophy, adrenal hypoplasia, hemophilia. At first, this could be obtained through invasive procedures such as amniocentesis and chorionic villus sampling, having a 1% risk of miscarriage. Since the discovery of cell-free fetal DNA (cffDNA) in maternal plasma, noninvasive prenatal testing permits the early diagnosis of fetal sex through analysis of cffDNA. However, the low amount of cffDNA relative to circulating maternal DNA requires highly sensitive molecular techniques in order to perform noninvasive prenatal diagnosis. In this context we employed droplet digital PCR (ddPCR) in order to evaluate the earliest possible fetal...
<div><p>The discovery of cell-free fetal DNA (cfDNA) circulating in the maternal blood has provided ...
Non-invasive prenatal diagnosis (NIPD) is based on fetal DNA analysis starting from a simple periphe...
Prenatal diagnosis in families affected by X-linked recessive disorders should ideally be limited to...
BACKGROUND: Fetal sex determination is useful for families at risk of X-linked disorders, such as Du...
Background and Purpose: Cell-free fetal DNA in maternal blood is a promising non-invasive alternativ...
Introduction: Prenatal diagnosis is testing for detection of diseases or conditions in a fetus...
Aim: The presence of circulatory cell-free fetal DNA in maternal plasma has found new applications i...
Enhancement of DNA detection assays increase the use of non-invasive prenatal diagnosis that is cons...
Free foetal DNA in maternal blood during early pregnancy is an ideal source of foetal genetic materi...
Background: The passage of nucleated cells between mother and fetus is well recognized (Lo et al., 1...
AbstractBackgroundThe passage of nucleated cells between mother and fetus is well recognized (Lo et ...
Objective To assess the viability of the early diagnosis of fetal gender in material plasma before 7...
Copyright © 2013 Elena Ordoñez et al.This is an open access article distributed under the Creative ...
Analysis of fetalDNA in maternal plasma has recently been introduced as a newmethod for noninvasive...
The discovery of cell-free fetal DNA (cfDNA) circulating in the maternal blood has provided new oppo...
<div><p>The discovery of cell-free fetal DNA (cfDNA) circulating in the maternal blood has provided ...
Non-invasive prenatal diagnosis (NIPD) is based on fetal DNA analysis starting from a simple periphe...
Prenatal diagnosis in families affected by X-linked recessive disorders should ideally be limited to...
BACKGROUND: Fetal sex determination is useful for families at risk of X-linked disorders, such as Du...
Background and Purpose: Cell-free fetal DNA in maternal blood is a promising non-invasive alternativ...
Introduction: Prenatal diagnosis is testing for detection of diseases or conditions in a fetus...
Aim: The presence of circulatory cell-free fetal DNA in maternal plasma has found new applications i...
Enhancement of DNA detection assays increase the use of non-invasive prenatal diagnosis that is cons...
Free foetal DNA in maternal blood during early pregnancy is an ideal source of foetal genetic materi...
Background: The passage of nucleated cells between mother and fetus is well recognized (Lo et al., 1...
AbstractBackgroundThe passage of nucleated cells between mother and fetus is well recognized (Lo et ...
Objective To assess the viability of the early diagnosis of fetal gender in material plasma before 7...
Copyright © 2013 Elena Ordoñez et al.This is an open access article distributed under the Creative ...
Analysis of fetalDNA in maternal plasma has recently been introduced as a newmethod for noninvasive...
The discovery of cell-free fetal DNA (cfDNA) circulating in the maternal blood has provided new oppo...
<div><p>The discovery of cell-free fetal DNA (cfDNA) circulating in the maternal blood has provided ...
Non-invasive prenatal diagnosis (NIPD) is based on fetal DNA analysis starting from a simple periphe...
Prenatal diagnosis in families affected by X-linked recessive disorders should ideally be limited to...