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PMID: 6745944 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Prenatal identification of a deleted Y chromosome by cytogenetics and a Y-specific repetitive DNA probe.

Human genetics ·Vol. 67 ·No. 2 ·1984-00-00 ·Pages 222-4

Disteche C, Luthy D, Haslam DB, Hoar D

Abstract

A very small sex chromosome was identified prenatally as a Y chromosome by using molecular hybridization in conjunction with conventional cytogenetics techniques. The combination of R-banding, Q-banding, distamycin-DAPI staining suggested that the chromosome might be a de novo deletion of the Y chromosome as the father's Y chromosome was normal. Restriction enzyme analysis of amniotic fluid cell DNA using a Y chromosome repetitive probe confirmed the origin of this chromosome.

MeSH Terms
Adult Amniotic Fluid/analysis Chromosome Banding Chromosome Deletion DNA/analysis Female Humans Infant, Newborn Male Pregnancy Prenatal Diagnosis Sex Chromosome Aberrations/diagnosis Y Chromosome
Chemicals
DNA
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Disteche C
Luthy D
Haslam D B
Hoar D
References (14)
14 references, click to expand
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Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
1984-00-00
Pages
222-4
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
Grants
NIA NIH HHS · AG 01751 · United States
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