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Genomic imprinting and genetic disorders in man



Genomic imprinting and genetic disorders in man



Trends in Genetics 5(10): 331-336



In a considerable number of genetic disorders in the human, the phenotypic expression of the disease can depend on maternal or paternal inheritance of the mutation. It is suggested that genomic imprinting, an epigenetic process that marks maternal and paternal chromosomes in mammals, is involved in such parental effects.

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Accession: 031578889

Download citation: RISBibTeXText

PMID: 2692240

DOI: 10.1016/0168-9525(89)90138-8



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