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Associations of MTHFR C677T and MTRR A66G Gene Polymorphisms with Metabolic Syndrome: A Case-Control Study in Northern China

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Liddle Syndrome: Review of the Literature and Description of a New Case

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A Microdeletion of Chromosome 9q33.3 Encompasses the Entire LMX1B Gene in a Chinese Family with Nail Patella Syndrome

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Next Generation Sequencing Approach in a Prenatal Case of Cardio-Facio-Cutaneus Syndrome

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