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. Case report: A 43-year-old woman underwent amniocentesis at 19 week...
Saved in:
Main Authors: | Meizi Zhang (Author), Yuehong Liang (Author), Hui Li (Author), Fengqin Xu (Author) |
---|---|
Format: | Book |
Published: |
Elsevier,
2024-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
PRADER-WILLI SYNDROME IDENTIFIED BY METHYLATION SPECIFIC MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION (MS-MLPA)
by: Simona Loredana Vasilache, et al.
Published: (2017) -
Prenatal diagnosis of a trisomy 7 mosaic case: CMA, CNV-seq, karyotyping, interphase FISH, and MS-MLPA, which technique to choose?
by: Xiaoyi Cong, et al.
Published: (2024) -
SINDROMUL PRADER WILLI IDENTIFICAT PRIN TEHNICA MS-MLPA (METHYLATION SPECIFIC MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION)
by: Simona Loredana Vasilache, et al.
Published: (2017) -
Prenatal diagnosis of low-level trisomy 15 mosaicism with a favorable outcome
by: Qi Zhao, et al.
Published: (2020) -
Prenatal diagnosis of trisomy 8 mosaicism
by: Chih-Ping Chen, et al.
Published: (2012)