Biblio
[Abnormal expression of PEX10 gene may be related to epilepsy associated with 1p36 copy number variations.]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015;32(1):6-10.
. [Analysis of a novel mutation of AR gene in a patient featuring mild androgen insensitivity syndrome]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014;31(2):219-22.
. Combinations of exonic deletions and rare mutations lead to misdiagnosis of propionic acidemia. Clin Chim Acta. 2019.
. Correlation between chromosomal distribution and embryonic findings on ultrasound in early pregnancy loss after IVF-embryo transfer. Hum Reprod. 2016.
. Differentiation of primordial germ cells from induced pluripotent stem cells of primary ovarian insufficiency. Hum Reprod. 2015.
. The dynamic changes of X chromosome inactivation during early culture of human embryonic stem cells. Stem Cell Res. 2016;17(1):84-92.
. Novel biallelic PCNT deletion causing microcephalic osteodysplastic primordial dwarfism type II with congenital heart defect. Sci China Life Sci. 2018.
. . .