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Publications by TT Nguyen

Whole Exome Sequencing in a Patient With Uniparental Disomy of Chromosome 2 and a Complex Phenotype

Clinical Genetics

English

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Causal Variants Screened by Whole Exome Sequencing in a Patient With Maternal Uniparental Isodisomy of Chromosome 10 and a Complicated Phenotype

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Paternal Uniparental Disomy of Chromosome 13

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Maternal Uniparental Disomy of Chromosome 20

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Maternal Uniparental Disomy of Chromosome 22

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Osteosarcoma in a Patient With Pseudohypoparathyroidism Type 1b Due to Paternal Uniparental Disomy of Chromosome 20q

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