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BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

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  • 21. Autosomal trisomy in a chimpanzee: resemblance to Down's syndrome.
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  • 23. [Chromosome aberrations in Langdon-Down's disease].
    Mieler W
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  • 26. [DOUBLE ANEUPLOIDY (TRISOMY 21 AND XXY) IN AN INFANT].
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  • 27. [THE PRINCIPLES OF FAMILIAL MONGOLISM].
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    [No Abstract]   [Full Text] [Related]  

  • 28. [RARE COMBINATION OF CHROMOSOME ABNORMALITIES].
    VAN WIJCK
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  • 29. [Genetic advice in Down's syndrome].
    Mikkelsen M
    Nord Med; 1971 Apr; 85(16):515. PubMed ID: 4252403
    [No Abstract]   [Full Text] [Related]  

  • 30. [Down's syndrome. Mongolism, trisomy 21].
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    [No Abstract]   [Full Text] [Related]  

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    [No Abstract]   [Full Text] [Related]  

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