Publications by authors named "Yun-Bi Lin"

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Nonsense Variant in the β-Spectrin Gene Causing Hereditary Spherocytosis Identified by Whole-Exome Sequencing in a Child.
Ai- Yang, Ti-Long Huang, Chun-Yan Song, Zu-Gang Xiao, Yun-Bi Lin

Hemoglobin· November 2025

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A splice mutation in gene in the patient with recurrent epistaxis and nasal vascular malformation.
Zhong-Yu Shi, Qing-Ling Lei, Shao-Qin Duan, Yan Zhou, Ting-Ting Cui, Yun-Bi Lin

Platelets· December 2024

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Gene Mutation Spectrum of Thalassemia Among Children in Yunnan Province.
Ti-Long Huang, Tian-Yao Zhang, Chun-Yan Song, Yun-Bi Lin, Bao-Hua Sang, Qing-Ling Lei

Front Pediatr· April 2020

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A de novo ANK1 mutation associated to hereditary spherocytosis: a case report.
Ti-Long Huang, Bao-Hua Sang, Qing-Ling Lei, Chun-Yan Song, Yun-Bi Lin

BMC Pediatr· February 2019

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