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Journal article

Rare chromosomal, genetic, and epigenetic-related risks associated with infertility treatment.

Abstract:

This article reviews the rarer chromosomal, genetic, and epigenetic-related risks of adverse child outcomes associated with infertility and its treatment. Excess structural chromosomal anomalies have been found in both male and female partners undergoing infertility treatment, and these risk direct transmission to offspring. Microdeletions of the Y-chromosome associated with male infertility have been transmitted to sons following treatment with intracytoplasmic sperm injection. It is thus po...

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Publication status:
Published

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Publisher copy:
10.1016/j.siny.2014.04.005

Authors


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Institution:
University of Oxford
Division:
MSD
Department:
Nuffield Department of Population Health
Sub department:
NPEU
Role:
Author
Journal:
Seminars in fetal and neonatal medicine
Volume:
19
Issue:
4
Pages:
250-253
Publication date:
2014-08-01
DOI:
EISSN:
1878-0946
ISSN:
1744-165X
Source identifiers:
469555
Language:
English
Keywords:
Pubs id:
pubs:469555
UUID:
uuid:6736c92a-6eb4-4485-a31e-58d397d5c953
Local pid:
pubs:469555
Deposit date:
2015-01-02

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