Xiumin Y. Wang

1678 Dongfang Road
Dongfang, 200127, China

Last Updated: 09/26/2026

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Found 55 publications

Clinical characteristics and genetic analysis of a child with Dyggve-Melchior-Clausen syndrome due to variant of DYM gene

Clinical characteristics and genetic analysis of a child with Dyggve-Melchior-Clausen syndrome due to variant of DYM gene

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

Published: June 24, 2026

Phenotypic and genotypic characteristics of pediatric patients with neurofibromatosis type 1: a 12-year single-center cohort study.

Phenotypic and genotypic characteristics of pediatric patients with neurofibromatosis type 1: a 12-year single-center cohort study.

Journal: World journal of pediatrics : WJP

Published: March 06, 2026

Pediatric X-linked adrenoleukodystrophy: phenotypes, variants, and HSCT outcomes.

Pediatric X-linked adrenoleukodystrophy: phenotypes, variants, and HSCT outcomes.

Journal: European journal of pediatrics

Published: February 15, 2026

Clinical delineation and genotype-phenotype correlation of 84 pediatric patients with Cornelia de Lange syndrome: insights from a single-center Chinese study.

Clinical delineation and genotype-phenotype correlation of 84 pediatric patients with Cornelia de Lange syndrome: insights from a single-center Chinese study.

Journal: European journal of pediatrics

Published: January 23, 2026

Clinical features and variant spectrum of FGFR3-related disorders

Clinical features and variant spectrum of FGFR3-related disorders

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

Published: October 22, 2025

Clinical and genetic spectrum of pediatric mitochondrial disorders in China: insights from a 47-case genetically confirmed cohort.

Clinical and genetic spectrum of pediatric mitochondrial disorders in China: insights from a 47-case genetically confirmed cohort.

Journal: Orphanet journal of rare diseases

Published: September 13, 2025

Alström syndrome: a cross-sectional and follow-up study of 127 patients in China, highlighting genetic variant spectrum and cardiac features.

Alström syndrome: a cross-sectional and follow-up study of 127 patients in China, highlighting genetic variant spectrum and cardiac features.

Journal: Orphanet journal of rare diseases

Published: June 10, 2025

Final height prediction of girls at menarche: a combined model using left hand and wrist bone age, knee radiomic scores, and clinical characteristics.

Final height prediction of girls at menarche: a combined model using left hand and wrist bone age, knee radiomic scores, and clinical characteristics.

Journal: World journal of pediatrics : WJP

Published: June 03, 2025

Alström syndrome in China: epidemiologic trends, geographic distribution, and clinical-socioeconomic profiles under innovative care models.

Alström syndrome in China: epidemiologic trends, geographic distribution, and clinical-socioeconomic profiles under innovative care models.

Journal: BMC pediatrics

Published: May 27, 2025

Age-related heterogeneity of type 1 diabetes mellitus in children: a single-center retrospective study.

Age-related heterogeneity of type 1 diabetes mellitus in children: a single-center retrospective study.

Journal: World journal of pediatrics : WJP

Published: May 14, 2025

Cardiovascular phenotypes of children and adolescents with Turner syndrome from a single-center cohort study.

Cardiovascular phenotypes of children and adolescents with Turner syndrome from a single-center cohort study.

Journal: Orphanet journal of rare diseases

Published: February 09, 2025

Correction: A novel ARCN1 splice-site variant in a Chinese girl with central precocious puberty, intrauterine growth restriction, microcephaly, and microretrognathia.

Correction: A novel ARCN1 splice-site variant in a Chinese girl with central precocious puberty, intrauterine growth restriction, microcephaly, and microretrognathia.

Journal: BMC pediatrics

Published: February 01, 2025

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Last Updated: 09/26/2026