Biyun Feng
1678 Dongfang Road
Dongfang, 200127, China
Dongfang, 200127, China
Last Updated: 09/26/2026
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Found 12 publications
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 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
Jordan syndrome due to PPP2R5D gene mutation: a report of two pediatric cases and literature review.
Jordan syndrome due to PPP2R5D gene mutation: a report of two pediatric cases and literature review.
Journal: Translational pediatrics
Published: July 18, 2025
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
A novel ARCN1 splice-site variant in a Chinese girl with central precocious puberty, intrauterine growth restriction, microcephaly, and microretrognathia.
Journal: BMC pediatrics
Published: September 27, 2024
Identification of a child with Teebi hypertelorism syndrome 1 due to variant of SPECC1L gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 02, 2023
A novel heterozygous variant of FOXJ1 in a Chinese female with primary ciliary dyskinesia and hydrocephalus: A case report and literature review.
Journal: Molecular genetics & genomic medicine
Published: March 28, 2023
Molecular and phenotypic spectrum of cardio-facio-cutaneous syndrome in Chinese patients.
Journal: Orphanet journal of rare diseases
Published: September 28, 2022
A novel CEP57 variant associated with mosaic variegated aneuploidy syndrome in a Chinese female presenting with short stature, microcephaly, brachydactyly, and small teeth.
Journal: Molecular genetics & genomic medicine
Published: November 26, 2021
Molecular and Phenotypic Expansion of Alström Syndrome in Chinese Patients.
Journal: Frontiers in genetics
Published: November 04, 2021
A novel homozygous variant of COL2A1 in a Chinese male with type II collagenopathy: a case report.
Journal: BMC medical genomics
Published: January 01, 2021
Showing 1-12 of 12
Last Updated: 09/26/2026