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Prenatal identification of a Y-chromosome deletion by Y-specific single copy DNA probes.

作者信息

Gilgenkrantz S, Droulle P, Seboun E, Casanova M, Schweitzer M, Goosens M, Fellous M

出版信息

Prenat Diagn. 1986 Jul-Aug;6(4):307-11. doi: 10.1002/pd.1970060412.

DOI:10.1002/pd.1970060412
PMID:3748996
Abstract

A sex chromosome deletion was identified in the course of prenatal diagnosis for maternal age. Ultrasound pictures revealed male fetal sex and a comparison with the father's Y chromosome suggested that the altered chromosome might be a de novo deletion of the Y chromosome. DNA hybridization with five human Y-specific probes shows that, among the Y-specific sequences recognized by the probes, only two of them are absent. The normal infant, at birth, was mosaic 46, XYq-/46,XY.

摘要

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