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Chromosome 16 Duplication Raises Risk Of Extreme Thinness Spectrum

Chromosome 16 Duplication Raises Risk Of Extreme Thinness Spectrum


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Chromosome 16 Duplication Raises Risk Of Extreme Thinness Spectrum

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Only Subset Of Chromosome 16 Variants Linked To Autism Spectrum

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16p112 Duplications Grch37hg19 Region On Chromosome 16p112 The

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