Fetal anomalies produced subsequent to treatment of zygotes with ethylene oxide or ethyl methanesulfonate are not likely due to the usual genetic causes

Author:

Katoh M.,Cacheiro N.L.A.,Cornett C.V.,Cain K.T.,Rutledge J.C.,Generoso W.M.

Publisher

Elsevier BV

Subject

Health, Toxicology and Mutagenesis,Genetics,Molecular Biology

Reference18 articles.

1. Midgestational abnormalities associated with in vitro preimplantation N-methyl-N-nitrosourea exposure with subsequent transfer to surrogate mothers;Bossert,1985

2. Fate and metabolism of some mutagenic alkylating agents in the mouse, I. Ethyl methylsulfonate and methyl methanesulfonate at sublethal dose in hybrid males;Cumming;Mutation Res.,1970

3. Dominant-lethal mutations and heritable translocations in mice;Generoso,1984

4. Exposure of female mice to ethylene oxide within hours after mating leads to fetal malformation and death;Generoso;Mutation Res.,1987

5. Mutagen-induced fetal anomalies and death following treatment of females within hours after mating;Generoso;Mutation Res.,1988

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