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Prenatal diagnosis with biotinylated chromosome specific probes.

作者信息

Guyot B, Bazin A, Sole Y, Julien C, Daffos F, Forestier F

机构信息

Centre de Diagnostic Prenatal et de Foetologie, Institut de Puériculture, Paris, France.

出版信息

Prenat Diagn. 1988 Sep;8(7):485-93. doi: 10.1002/pd.1970080703.

DOI:10.1002/pd.1970080703
PMID:3222216
Abstract

We have used a Y-chromosome specific DNA probe in a controlled study to determine the presence of Y-chromosome material and to detect numerical abnormalities in uncultured amniotic fluid cells by fluorescent hybridization. Using this non-radioactive method, we correctly predicted fetal sex within 48 h in all but 3 of 54 cases and identified an XYY syndrome. The technique was previously tested with no false-positive or false-negative results on cultured interphase or metaphase nuclei of fetal fibroblasts and adult T-lymphocytes. Fluorescent in situ hybridization was applied to long-term fixed cytogenetic preparations up to 44 months old and was shown to be reliable.

摘要

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引用本文的文献

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Maternal cell contamination in amniotic fluid samples as a consequence of the sampling technique.由于采样技术导致羊水样本中出现母源细胞污染。
Hum Genet. 1994 Feb;93(2):121-4. doi: 10.1007/BF00210594.
2
Interphase cytogenetics.
Neurochem Res. 1990 Apr;15(4):467-74. doi: 10.1007/BF00969934.
3
New rapid test for prenatal detection of trisomy 21 (Down's syndrome): preliminary report.用于产前检测21三体综合征(唐氏综合征)的新型快速检测方法:初步报告。
BMJ. 1992 Jun 13;304(6841):1536-9. doi: 10.1136/bmj.304.6841.1536.