Author [ Title] Type Year
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[Abnormal expression of PEX10 gene may be related to epilepsy associated with 1p36 copy number variations.].Zhonghua Yi Xue Yi Chuan Xue Za Zhi32, 6-10.(2015).
[Analysis of a novel mutation of AR gene in a patient featuring mild androgen insensitivity syndrome].Zhonghua Yi Xue Yi Chuan Xue Za Zhi31, 219-22.(2014).
Combinations of exonic deletions and rare mutations lead to misdiagnosis of propionic acidemia.Clin Chim Acta.(2019).
Differentiation of primordial germ cells from induced pluripotent stem cells of primary ovarian insufficiency.Hum Reprod.(2015).
Novel biallelic PCNT deletion causing microcephalic osteodysplastic primordial dwarfism type II with congenital heart defect.Sci China Life Sci.(2018).