Xiaobin Y. Wang
1616 Yanxiang Road
Xi'an, China
Xi'an, China
Last Updated: 09/26/2026
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Found 9 publications
In Silico Fragment Size Selection for Enhanced Fetal Fraction and Abnormality Origin Discernment Using Pair-End Sequencing of Maternal Plasma DNA.
Journal: Journal of clinical laboratory analysis
Published: June 24, 2025
A case of neonatal complete Kawasaki disease
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: April 07, 2022
Clinical application of NGS-based SNP haplotyping for PGT-M of methylmalonic acidemia.
Journal: Systems biology in reproductive medicine
Published: December 16, 2021
Allelic dropout in PAH affecting the results of genetic diagnosis in phenylketonuria.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: May 13, 2021
Mutation analysis of the phenylalanine hydroxylase gene and prenatal diagnosis of phenylketonuria in Shaanxi, China.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: December 02, 2016
MLL1 promotes cervical carcinoma cell tumorigenesis and metastasis through interaction with β-catenin.
Journal: OncoTargets and therapy
Published: November 16, 2016
Mutations of the phenylalanine hydroxylase gene in phenylketonuria patients from Shaanxi
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: February 11, 2014
microRNA-151-3p regulates slow muscle gene expression by targeting ATP2a2 in skeletal muscle cells.
Journal: Journal of cellular physiology
Published: January 27, 2014
Showing 1-9 of 9
Last Updated: 09/26/2026