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The length of Y-chromosomal sequence reads in noninvasive prenatal testing reflect allogeneic bone marrow transplant.

作者信息

Balslev-Harder Marie, Jørgensen Finn Stener, Kjaergaard Susanne, Johansen Peter

机构信息

Chromosome Laboratory, Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Denmark.

Fetal Medicine Unit, Department of Obstetrics and Gynecology, Copenhagen University Hospital Hvidovre, Denmark.

出版信息

Prenat Diagn. 2017 Aug;37(8):843-845. doi: 10.1002/pd.5081. Epub 2017 Jul 10.

DOI:10.1002/pd.5081
PMID:28585331
Abstract
摘要

相似文献

1
The length of Y-chromosomal sequence reads in noninvasive prenatal testing reflect allogeneic bone marrow transplant.无创产前检测中Y染色体序列读数的长度反映了异基因骨髓移植情况。
Prenat Diagn. 2017 Aug;37(8):843-845. doi: 10.1002/pd.5081. Epub 2017 Jul 10.
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Endothelial cells but not epithelial cells or cardiomyocytes are partially replaced by donor cells after allogeneic bone marrow and stem cell transplantation.在同种异体骨髓和干细胞移植后，内皮细胞而非上皮细胞或心肌细胞会被供体细胞部分替代。
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The detection of wt-1 transcripts is not associated with an increased leukemic relapse rate in patients with acute leukemia after allogeneic bone marrow or peripheral blood stem cell transplantation.在接受异基因骨髓或外周血干细胞移植的急性白血病患者中，wt-1转录本的检测与白血病复发率升高无关。
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Detection of Y chromosome material in a 46,XX male with SRY translocation: novel application of cell-free fetal DNA testing.在一名具有SRY易位的46,XX男性中检测Y染色体物质：游离胎儿DNA检测的新应用
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[Origin of mesenchymal stem cells in bone marrow of patients after allogeneic stem cell transplantation].
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引用本文的文献

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Noninvasive prenatal screening in a pregnant woman with a history of stem cell transplant from a male donor: A case report and literature review.男性供者干细胞移植史孕妇的无创性产前筛查：病例报告及文献复习。
Mol Genet Genomic Med. 2024 Jun;12(6):e2479. doi: 10.1002/mgg3.2479.
2
Chromosome Y as a marker for sex discrepancies in patients with organ transplants: a case report.染色体Y作为器官移植患者性别差异的标志物：一例报告
Mol Cytogenet. 2021 Jan 6;14(1):3. doi: 10.1186/s13039-020-00523-0.
3
Cherchez la femme: maternal incidental findings can explain discordant prenatal cell-free DNA sequencing results.
寻找病因：母体偶然发现的异常可解释不一致的产前游离 DNA 测序结果。
Genet Med. 2018 Sep;20(9):910-917. doi: 10.1038/gim.2017.219. Epub 2017 Dec 7.