Ding-wen Wu

Hangzhou, China

Last Updated: 09/26/2026

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Found 11 publications

Clinical and genetic features of 5 neonates with centronuclear myopathy caused by MTM1 gene variation

Clinical and genetic features of 5 neonates with centronuclear myopathy caused by MTM1 gene variation

Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics

Published: September 17, 2025

Comprehensive newborn screening for severe combined immunodeficiency, X-linked agammaglobulinemia, and spinal muscular atrophy: the Chinese experience.

Comprehensive newborn screening for severe combined immunodeficiency, X-linked agammaglobulinemia, and spinal muscular atrophy: the Chinese experience.

Journal: World journal of pediatrics : WJP

Published: January 25, 2024

Successful treatment of retinopathy of prematurity in oculocutaneous albinism with OCA2 variants: a case report and review of literature.

Successful treatment of retinopathy of prematurity in oculocutaneous albinism with OCA2 variants: a case report and review of literature.

Journal: BMC pediatrics

Published: October 22, 2023

A multicenter prospective study of next-generation sequencing-based newborn screening for monogenic genetic diseases in China.

A multicenter prospective study of next-generation sequencing-based newborn screening for monogenic genetic diseases in China.

Journal: World journal of pediatrics : WJP

Published: May 10, 2022

Surgical management and molecular diagnosis of persistent Müllerian duct syndrome in Chinese patients.

Surgical management and molecular diagnosis of persistent Müllerian duct syndrome in Chinese patients.

Journal: Asian journal of andrology

Published: November 23, 2021

Application of next generation sequencing in the screening of monogenic diseases in China, 2021: a consensus among Chinese newborn screening experts.

Application of next generation sequencing in the screening of monogenic diseases in China, 2021: a consensus among Chinese newborn screening experts.

Journal: World journal of pediatrics : WJP

Published: October 04, 2021

FMR1 allele frequencies in 51,000 newborns: a large-scale population study in China.

FMR1 allele frequencies in 51,000 newborns: a large-scale population study in China.

Journal: World journal of pediatrics : WJP

Published: June 04, 2021

A novel TFG c.793C>G mutation in a Chinese pedigree with Charcot-Marie-Tooth disease 2.

A novel TFG c.793C>G mutation in a Chinese pedigree with Charcot-Marie-Tooth disease 2.

Journal: Brain and behavior

Published: February 27, 2020

Methylation analysis of CpG island DNA of FMR1 gene in the fragile X syndrome

Methylation analysis of CpG island DNA of FMR1 gene in the fragile X syndrome

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: March 02, 2013

Relationship between 22q11 microdeletion syndrome and congenital heart disease

Relationship between 22q11 microdeletion syndrome and congenital heart disease

Journal: Zhonghua xin xue guan bing za zhi

Published: November 18, 2011

Clinical and genetic analysis of a pedigree of Kennedy disease

Clinical and genetic analysis of a pedigree of Kennedy disease

Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences

Published: October 11, 2011

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Last Updated: 09/26/2026