Results 1 to 10 of about 5,849,237 (150)
Objective: We present mosaic trisomy 15 at amniocentesis. Materials and methods: A 41-year-old woman underwent amniocentesis at 16 weeks of gestation because of an abnormal non-invasive prenatal testing (NIPT) result suspicious of trisomy 15 ...
Chih-Ping Chen +10 more
doaj +4 more sources
Objective: We present low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a positive non-invasive prenatal testing (NIPT) result suspicious of trisomy 13, a chorionic villus sampling (CVS) result of mosaic trisomy 13, cytogenetic ...
Gwo-Chin Ma +2 more
exaly +4 more sources
Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review [PDF]
Objective: To present prenatal diagnosis of mosaic trisomy 15 at amniocentesis. Materials and methods: A 37-year-old woman underwent amniocentesis at 17 weeks of gestation because of advanced maternal age.
Chih-Ping Chen +6 more
doaj +4 more sources
Objective: We present prenatal diagnosis of mosaic trisomy 15 in a pregnancy with a favorable outcome. Case report: A 33-year-old, primigravid woman underwent amniocentesis at 19 weeks of gestation because non-invasive prenatal testing (NIPT) revealed ...
Chih-Ping Chen +9 more
doaj +3 more sources
Objective: We present low-level mosaic trisomy 15 without uniparental disomy (UPD) 15 in a pregnancy associated with cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes, a favorable fetal outcome and perinatal decrease of the ...
Chih-Ping Chen +7 more
doaj +3 more sources
Objective: To investigate the cause of a false-negative result in prenatal amniotic fluid karyotype analysis for a fetus with mosaic trisomy 15, and to propose a cytomolecular genetic strategy for detecting mosaicism in amniotic fluid.
Xiang Li +4 more
doaj +3 more sources
Use of the MS-MLPA assay in prenatal diagnosis of Prader–Willi syndrome with mosaic trisomy 15
Objective: We present a prenatal diagnosis strategy of using Methylation-Specific Multiplex Ligation-Dependent Probe Amplification (MS-MLPA) for the detection of maternal uniparental disomy 15/trisomy 15 (UPD(15) mat/T15) mosaicism.
Meizi Zhang +3 more
doaj +3 more sources
Objective: To inform clinicians of the first known case of a live born diagnosed with syndromic partial trisomy 15 and maternal uniparental disomy 15 resulting from a mosaic embryo transfer (MET).
Kamilla Schlade-Bartusiak, Ph.D. +7 more
doaj +1 more source
Trisomy 15 mosaicism: Challenges in prenatal diagnosis [PDF]
Keywords: trisomy 15 mosaicism; fetal mosaicism; chorionic villi; prenatal cytogenetics; SNP-array; uniparental ...
Silva, Marisa +9 more
openaire +3 more sources

