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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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C1q/TNF-Related Protein-9 Ameliorates Ox-LDL-Induced Endothelial Dysfunction via PGC-1α/AMPK-Mediated Antioxidant Enzyme Induction

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The 15q11.2 BP1–BP2 Microdeletion Syndrome: A Review

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Screening for Mutations in the TBX1 Gene on Chromosome 22q11.2 in Schizophrenia

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