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You searched for: Author/Creator Li, Miaoxin

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1. Cancer gene mutations in congenital pulmonary airway malformation patients. Issue 1 (4th February 2019)

4. De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca. (21st November 2017)

5. Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases. Issue 6 (20th December 2021)

6. Dysfunction of Myosin Light‐Chain 4 (MYL4) Leads to Heritable Atrial Cardiomyopathy With Electrical, Contractile, and Structural Components: Evidence From Genetically‐Engineered Rats. Issue 11 (28th October 2017)