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Can Liao

Showing results (221-230 of 262) with videos related to

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Prenatal Diagnosis|May 22, 2020
Whole-exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonographyTing-Ying Lei, Fang Fu, Ru Li, et al.
Inorganic Chemistry|December 11, 2025
Single-Determinant Ground State in Ce<sup>4+</sup> Imidophosphorane ComplexesHaruko Tateyama, Can Liao, Grant R Wilkinson, et al.
Journal of Cellular Biochemistry|January 22, 2020
All-trans-retinoid acid induces the differentiation of P19 cells into neurons involved in the PI3K/Akt/GSK3β signaling pathwayFang Fu, Lu-Shan Li, Ru Li, et al.
Annals of Hematology|February 11, 2025
An unusual transfusion-dependent hemoglobin H disease caused by a novel complex inverted duplication involving the α-globin regulatory elements and α-thalassemia--SEA deletionFan Jiang, Jieying Wu, Manqiu Yang, et al.
Prenatal Diagnosis|July 3, 2018
Early prenatal diagnosis of lysosomal storage disorders by enzymatic and molecular analysisDuan Li, Yunting Lin, Yonglan Huang, et al.
Prenatal Diagnosis|January 28, 2022
Prenatal exome sequencing in fetuses with callosal anomaliesTing-Ying Lei, Qin She, Fang Fu, et al.
Frontiers in Genetics|September 25, 2023
Exome sequencing improves genetic diagnosis of congenital orofacial cleftsShujuan Yan, Fang Fu, Ru Li, et al.
Frontiers in Genetics|October 3, 2022
Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencingFang Fu, Ru Li, Xiao Dang, et al.
Clinical Genetics|February 13, 2026
Novel Haplotype-Based Noninvasive Prenatal Diagnosis for Recessive Single-Gene Disorders: A Proof-of-Concept StudyChao Chen, Yaping Zhu, Lu Jiang, et al.
Frontiers in Genetics|May 25, 2023
Genetic diagnosis of fetal microcephaly at a single tertiary center in ChinaYou Wang, Fang Fu, Tingying Lei, et al.
Pageof 27

Showing results (221-230 of 262) with videos related to

Sort By:
Pageof 27
Prenatal Diagnosis|May 22, 2020
Whole-exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonographyTing-Ying Lei, Fang Fu, Ru Li, et al.
Inorganic Chemistry|December 11, 2025
Single-Determinant Ground State in Ce<sup>4+</sup> Imidophosphorane ComplexesHaruko Tateyama, Can Liao, Grant R Wilkinson, et al.
Journal of Cellular Biochemistry|January 22, 2020
All-trans-retinoid acid induces the differentiation of P19 cells into neurons involved in the PI3K/Akt/GSK3β signaling pathwayFang Fu, Lu-Shan Li, Ru Li, et al.
Annals of Hematology|February 11, 2025
An unusual transfusion-dependent hemoglobin H disease caused by a novel complex inverted duplication involving the α-globin regulatory elements and α-thalassemia--SEA deletionFan Jiang, Jieying Wu, Manqiu Yang, et al.
Prenatal Diagnosis|July 3, 2018
Early prenatal diagnosis of lysosomal storage disorders by enzymatic and molecular analysisDuan Li, Yunting Lin, Yonglan Huang, et al.
Prenatal Diagnosis|January 28, 2022
Prenatal exome sequencing in fetuses with callosal anomaliesTing-Ying Lei, Qin She, Fang Fu, et al.
Frontiers in Genetics|September 25, 2023
Exome sequencing improves genetic diagnosis of congenital orofacial cleftsShujuan Yan, Fang Fu, Ru Li, et al.
Frontiers in Genetics|October 3, 2022
Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencingFang Fu, Ru Li, Xiao Dang, et al.
Clinical Genetics|February 13, 2026
Novel Haplotype-Based Noninvasive Prenatal Diagnosis for Recessive Single-Gene Disorders: A Proof-of-Concept StudyChao Chen, Yaping Zhu, Lu Jiang, et al.
Frontiers in Genetics|May 25, 2023
Genetic diagnosis of fetal microcephaly at a single tertiary center in ChinaYou Wang, Fang Fu, Tingying Lei, et al.
Pageof 27