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Yunli Lai

Showing results (11-20 of 15) with videos related to

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Genes|April 3, 2021
Performance of Cell-Free DNA Screening for Fetal Common Aneuploidies and Sex Chromosomal Abnormalities: A Prospective Study from a Less Developed Autonomous Region in Mainland ChinaYunli Lai, Xiaofan Zhu, Sheng He, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 13, 2015
PAX8 pathogenic variants in Chinese patients with congenital hypothyroidismChunyun Fu, Rongyu Chen, Shujie Zhang, et al.
Molecular and Cellular Endocrinology|January 19, 2016
Thyroglobulin gene mutations in Chinese patients with congenital hypothyroidismXuyun Hu, Rongyu Chen, Chunyun Fu, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|June 11, 2019
A Cell-free DNA Barcode-Enabled Single-Molecule Test for Noninvasive Prenatal Diagnosis of Monogenic Disorders: Application to β-ThalassemiaXingkun Yang, Qinghua Zhou, Wanjun Zhou, et al.
Human Genetics|May 27, 2020
Low-pass genome sequencing: a validated method in clinical cytogeneticsMatthew Hoi Kin Chau, Huilin Wang, Yunli Lai, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Genes|April 3, 2021
Performance of Cell-Free DNA Screening for Fetal Common Aneuploidies and Sex Chromosomal Abnormalities: A Prospective Study from a Less Developed Autonomous Region in Mainland ChinaYunli Lai, Xiaofan Zhu, Sheng He, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 13, 2015
PAX8 pathogenic variants in Chinese patients with congenital hypothyroidismChunyun Fu, Rongyu Chen, Shujie Zhang, et al.
Molecular and Cellular Endocrinology|January 19, 2016
Thyroglobulin gene mutations in Chinese patients with congenital hypothyroidismXuyun Hu, Rongyu Chen, Chunyun Fu, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|June 11, 2019
A Cell-free DNA Barcode-Enabled Single-Molecule Test for Noninvasive Prenatal Diagnosis of Monogenic Disorders: Application to β-ThalassemiaXingkun Yang, Qinghua Zhou, Wanjun Zhou, et al.
Human Genetics|May 27, 2020
Low-pass genome sequencing: a validated method in clinical cytogeneticsMatthew Hoi Kin Chau, Huilin Wang, Yunli Lai, et al.
Pageof 2