The role of molecular mutation in recurrent euploidic abortion

P. G. McDonough

doi:10.1055/s-2007-1021351

The role of molecular mutation in recurrent euploidic abortion

P. G. McDonough

Physiology

Research output: Contribution to journal › Article › peer-review

8 Scopus citations

Abstract

The cause of euploidic embryonic loss in man is clearly the future challenge for developmental biologists and interested clinicians. The precise mutations that are embryonically lethal will have to be characterized and automated DNA-RNA screening techniques developed in order to take advantage of this information. The legacy of a decade of experimental recombinant molecular biology should ultimately provide the key to the critical human morphogenes and their mutant counterparts.

Original language	English (US)
Pages (from-to)	155-161
Number of pages	7
Journal	Seminars in Reproductive Endocrinology
Volume	6
Issue number	2
DOIs	https://doi.org/10.1055/s-2007-1021351
State	Published - 1988

ASJC Scopus subject areas

Endocrinology, Diabetes and Metabolism
Physiology
Reproductive Medicine
Endocrinology

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1055/s-2007-1021351

Cite this

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The role of molecular mutation in recurrent euploidic abortion

Abstract

ASJC Scopus subject areas

UN SDGs

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