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Chromosome imprinting and the mammalian X chromosome

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A Corrigendum to this article was published on 29 May 1975

Abstract

Chromosome imprinting is the process by which one of two genetically homologous chromosomes is predetermined to function differently from the other at a subsequent stage in development. In the coccid insects, imprinting occurs in the egg, at the time of fertilisation; it probably occurs at the same time and site in mammals, and possibly also in Sciara.

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Authors and Affiliations

  1. Microbiology and Pharmacology Laboratory and Centre for Theoretical Studies, Indian Institute of Science, Bangalore, 560012

    H. Sharat Chandra

  2. Department of Genetics, University of California, Berkeley, California, 94720

    Spencer W. Brown

Authors
  1. H. Sharat Chandra
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  2. Spencer W. Brown
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Additional information

The original article can be found online at https://doi.org/10.1038/255428a0

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Chandra, H., Brown, S. Chromosome imprinting and the mammalian X chromosome. Nature 253, 165–168 (1975). https://doi.org/10.1038/253165a0

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