Author

Xutao Hong

Institution: Wenzhou Central Hospital

Observed institution: Wenzhou Central Hospital

ORCID: 0000-0002-9971-8332

Observed ORCID: 0000-0002-9971-8332

OpenAlex ID: A5120968363

Targeted Carrier Screening for Thalassemia, Hereditary Deafness, and Spinal Muscular Atrophy: A Feasible Approach for Preventing Birth Defects in China's Community Healthcare System

2026 · Zhihui Wang, Wenjing Bai, et al. · Molecular Genetics & Genomic Medicine · 1

A Rare Case of Prenatal Short‐Rib Thoracic Dysplasia 11 Subtype With Compound Heterozygous Variants in the DYNC2I2 Gene: Presenting Polydactyly and Shortened Limbs

2026 · Zhihui Wang, Heqin Guan, et al. · Clinical Case Reports

Accelerated Identification and Preliminary Validation of a Pathogenic Missense Variant in the L1CAM Gene in a Pregnant Woman With Sonographic Anomalies Using AlphaMissense

2025 · Zhihui Wang, Xuna Shen, et al. · Molecular Genetics & Genomic Medicine

Works count: 3

Citation count: 1

H-index: 1

I10-index: