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Homo sapiens chromosome 19, GRCh38.p14 Primary Assembly

NCBI Reference Sequence: NC_000019.10

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  • Facies
    Facies
    The appearance of the face that is often characteristic of a disease or pathological condition, as the elfin facies of WILLIAMS SYNDROME or facies of DOWN SYNDROME. (Random Ho...<br/>Year introduced: 1996
    MeSH

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