The role of molecular mutation in recurrent euploidic abortion

P. G. McDonough

Research output: Contribution to journalArticle

8 Citations (Scopus)

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 languageEnglish (US)
Pages (from-to)155-161
Number of pages7
JournalSeminars in Reproductive Endocrinology
Volume6
Issue number2
StatePublished - Jan 1 1988

Fingerprint

Habitual Abortion
Molecular Biology
RNA
Mutation
DNA

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Physiology
  • Reproductive Medicine
  • Endocrinology

Cite this

The role of molecular mutation in recurrent euploidic abortion. / McDonough, P. G.

In: Seminars in Reproductive Endocrinology, Vol. 6, No. 2, 01.01.1988, p. 155-161.

Research output: Contribution to journalArticle

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