Biblio

Author Title [ Type(Asc)] Year
Filters: Author is Tan, Yueqiu  [Clear All Filters]
Journal Article
Qu S, Zhang Y, Yang X, Tan Y, Li M, Yang X, Zhou L, Chen D, Chen Y, Yan M, et al. The Setup and Application of Reference Material in Sequencing-Based Noninvasive Prenatal Testing. Gynecol Obstet Invest. 2021:1-9.
Xie P, Hu L, Tan Y, Gong F, Zhang S, Xiong B, Peng Y, Lu GXiu, Lin G. Retrospective analysis of meiotic segregation pattern and interchromosomal effects in blastocysts from inversion preimplantation genetic testing cycles. Fertil Steril. 2019.
Zhang S, Luo K, Cheng D, Tan Y, Lu C, He H, Gu Y, Lu G, Gong F, Lin G. The number of biopsied trophectoderm cells is likely to affect the implantation potential of blastocysts with poor trophectoderm quality. Fertil Steril. 2016.
Meng L, Tu C, Lu G, Lin G, Tan Y. Novel biallelic PCNT deletion causing microcephalic osteodysplastic primordial dwarfism type II with congenital heart defect. Sci China Life Sci. 2018.
Xie P, Ouyang Q, Leng L, Hu L, Cheng D, Tan Y, Lu G, Lin G. The dynamic changes of X chromosome inactivation during early culture of human embryonic stem cells. Stem Cell Res. 2016;17(1):84-92.
Leng L, Tan Y, Gong F, Hu L, Ouyang Q, Zhao Y, Lu G, Lin G. Differentiation of primordial germ cells from induced pluripotent stem cells of primary ovarian insufficiency. Hum Reprod. 2015.
Ouyang Y, Tan Y, Yi Y, Gong F, Lin G, Li X, Lu G. Correlation between chromosomal distribution and embryonic findings on ultrasound in early pregnancy loss after IVF-embryo transfer. Hum Reprod. 2016.
Wang H, Meng L, Li W, Du J, Tan Y, Gong F, Lu G, Lin G, Zhang Q. Combinations of exonic deletions and rare mutations lead to misdiagnosis of propionic acidemia. Clin Chim Acta. 2019.
Zhang Y, Li W, Du J, Cao W, Lu G, Tan Y. [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.
Luo S, He W, Liao Y, Tang W, Li X, Hu L, Du J, Zhang Q, Tan Y, Lin G, et al. [Analysis and prenatal diagnosis of FMR1 gene mutations among patients with unexplained mental retardation]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021;38(5):439-445.
Zhang Y, Xu F, Tan Y, Hu J, Wang H. [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.