Objective: The coexistence of maternal malignancy and pregnancy has received increasing attention in Noninvasive prenatal testing (NIPT) studies. Malignancy in pregnant women potentially affects the copy number variation (CNV) profile in NIPT results. Only one case of hematologic cancer has been reported in a Hong-Kong pregnant women, and solid tumors have never been reported in pregnant Chinese women. Case report: The patients with dysgerminoma and cervical cancer showed aberrant chromosomal aneuploidies in NIPT and concordant patterns of genome disruption in tumor tissues. The genomic aberrations in the gastric cancer patient had similar copy number variation pattern of gastric cancer. Conclusion: The findings in this study and the litera...
Abstract Background We aimed to evaluate the clinical value of copy number variation-sequencing (CNV...
Our goal was to test the hypothesis that inter-individual genomic copy number variation in control s...
Contains fulltext : 153103.pdf (publisher's version ) (Closed access)Noninvasive p...
PURPOSE: Noninvasive prenatal testing (NIPT) for fetal aneuploidy screening using cell-free DNA deri...
PURPOSE:Noninvasive prenatal testing (NIPT) for fetal aneuploidy screening using cell-free DNA deriv...
PURPOSE: Noninvasive prenatal screening (NIPS) using genome sequencing also reveals maternal copy-nu...
IMPORTANCE Noninvasive prenatal testing (NIPT) for fetal aneuploidy by scanning cell-free fetal DNA ...
BACKGROUND: Non-invasive prenatal testing (NIPT) identifies fetal aneuploidy by sequencing cell-free...
Background: Non-invasive prenatal testing (NIPT) is currently offered for the detection of Trisomy 2...
Abstract We present a clinical case where a complex abnormal non‐invasive prenatal test (NIPT) resul...
Analyses of cell-free fetal DNA (cff-DNA) from maternal plasma using massively parallel sequencing e...
Our goal was to test the hypothesis that inter-individual genomic copy number variation in control s...
Background: Low-pass genome sequencing (GS) detects clinically significant copy number variants (CNV...
Objective: Amniocentesis, chorionic villi sampling and first trimester combined testing are able to ...
BACKGROUND: Numerous publications have reported the incidental detection of occult malignancies upon...
Abstract Background We aimed to evaluate the clinical value of copy number variation-sequencing (CNV...
Our goal was to test the hypothesis that inter-individual genomic copy number variation in control s...
Contains fulltext : 153103.pdf (publisher's version ) (Closed access)Noninvasive p...
PURPOSE: Noninvasive prenatal testing (NIPT) for fetal aneuploidy screening using cell-free DNA deri...
PURPOSE:Noninvasive prenatal testing (NIPT) for fetal aneuploidy screening using cell-free DNA deriv...
PURPOSE: Noninvasive prenatal screening (NIPS) using genome sequencing also reveals maternal copy-nu...
IMPORTANCE Noninvasive prenatal testing (NIPT) for fetal aneuploidy by scanning cell-free fetal DNA ...
BACKGROUND: Non-invasive prenatal testing (NIPT) identifies fetal aneuploidy by sequencing cell-free...
Background: Non-invasive prenatal testing (NIPT) is currently offered for the detection of Trisomy 2...
Abstract We present a clinical case where a complex abnormal non‐invasive prenatal test (NIPT) resul...
Analyses of cell-free fetal DNA (cff-DNA) from maternal plasma using massively parallel sequencing e...
Our goal was to test the hypothesis that inter-individual genomic copy number variation in control s...
Background: Low-pass genome sequencing (GS) detects clinically significant copy number variants (CNV...
Objective: Amniocentesis, chorionic villi sampling and first trimester combined testing are able to ...
BACKGROUND: Numerous publications have reported the incidental detection of occult malignancies upon...
Abstract Background We aimed to evaluate the clinical value of copy number variation-sequencing (CNV...
Our goal was to test the hypothesis that inter-individual genomic copy number variation in control s...
Contains fulltext : 153103.pdf (publisher's version ) (Closed access)Noninvasive p...