Works by Feng, Biyun

Results: 9

Converting Agroforestry Biowaste into Stable Near-Natural Chars via Hydrothermal Humification and Pyrolysis for Immobilizing Plasticizer.

Published in:

Agriculture; Basel, 2025, v. 15, n. 11, p. 1177, doi. 10.3390/agriculture15111177

By:

Xue, Tao;
Li, Yi;
Chen, Zimo;
Kong, Chao;
Feng, Biyun;
Zhu, Changyin;
Zhang, Yinlong;
Xue, Jianming;
Cheng, Hu

Publication type:

Article

Molecular and Phenotypic Expansion of Alström Syndrome in Chinese Patients.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.808919

By:

Zhang, Qianwen;
Ding, Yu;
Feng, Biyun;
Tang, Yijun;
Chen, Yao;
Wang, Yirou;
Chang, Guoying;
Liu, Shijian;
Wang, Jian;
Li, Qian;
Fu, Lijun;
Wang, Xiumin

Publication type:

Article

A novel heterozygous variant of FOXJ1 in a Chinese female with primary ciliary dyskinesia and hydrocephalus: A case report and literature review.

Published in:

Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 9, p. 1, doi. 10.1002/mgg3.2235

By:

Gao, Shiyang;
Zhang, Qianwen;
Feng, Biyun;
Gu, Shili;
Li, Zhiying;
Sun, Lianping;
Yao, Ru‐en;
Yu, Tingting;
Ding, Yu;
Wang, Xiumin

Publication type:

Article

A novel CEP57 variant associated with mosaic variegated aneuploidy syndrome in a Chinese female presenting with short stature, microcephaly, brachydactyly, and small teeth.

Published in:

Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 6, p. 1, doi. 10.1002/mgg3.1951

By:

Feng, Biyun;
Chang, Guoying;
Zhang, Qianwen;
Li, Xin;
Tang, Yijun;
Gu, Shili;
Wang, Yirou;
Wang, Jian;
Wang, Xiumin

Publication type:

Article

Genetic variants of ABCC8 and clinical manifestations in eight Chinese children with hyperinsulinemic hypoglycemia.

Published in:

BMC Endocrine Disorders, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12902-023-01527-8

By:

Chang, Guoying;
Ying, Lingwen;
Zhang, Qianwen;
Feng, Biyun;
Yao, Ruen;
Ding, Yu;
Li, Juan;
Huang, Xiaodong;
Shen, Yongnian;
Yu, Tingting;
Wang, Jian;
Wang, Xiumin

Publication type:

Article

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

Published in:

2025

By:

Chang, Guoying;
Yang, Fan;
Ying, Lingwen;
Zhang, Qianwen;
Feng, Biyun;
Chen, Yao;
Ding, Yu;
Yu, Tingting;
Yao, Ruen;
Lin, Kana;
Li, Juan;
Wang, Xiumin

Publication type:

Correction Notice

Molecular and phenotypic spectrum of cardio-facio-cutaneous syndrome in Chinese patients.

Published in:

Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02878-0

By:

Feng, Biyun;
Li, Xin;
Zhang, Qianwen;
Wang, Yirou;
Gu, Shili;
Yao, Ru-en;
Li, Zhiying;
Gao, Shiyang;
Chang, Guoying;
Li, Qun;
Li, Niu;
Fu, Lijun;
Wang, Jian;
Wang, Xiumin

Publication type:

Article

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

Published in:

BMC Pediatrics, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12887-024-05329-2

By:

Chang, Guoying;
Yang, Fan;
Ying, Lingwen;
Zhang, Qianwen;
Feng, Biyun;
Chen, Yao;
Ding, Yu;
Yu, Tingting;
Yao, Ruen;
Lin, Kana;
Li, Juan;
Wang, Xiumin

Publication type:

Article

A novel homozygous variant of COL2A1 in a Chinese male with type II collagenopathy: a case report.

Published in:

BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01048-0

By:

Zhang, Qianwen;
Yao, Ruen;
Li, Qun;
Li, Xin;
Feng, Biyun;
Chang, Guoying;
Wang, Jian;
Wang, Xiumin

Publication type:

Article