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Molecular Genetics & Gen…
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It’s in Our Blood: A Glimpse of Personalized Medicine: Trends in Molecular Medicine
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A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia,Mole…

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HPDL mutations identified by exome sequencing are associated with infant neurodevelopmental ...
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Genetics Basics: Introduction to Genetics

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Cover,Molecular Genetics & Genomic Medicine - X-MOL
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Global research on Fabry's disease: De…
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Human Genome Project timeline

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Okur‐Chung neurodevelopmental syndrome: Implications for phenotype and genotype expansion ...

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