Author

B Q Yu

Observed name: Baofeng Yu

OpenAlex ID: A5079519604

Whole exome sequencing identifies a novel missense FBN2 mutation co-segregating in a four-generation Chinese family with congenital contractural arachnodactyly

2016 · Xingping Guo, Chunying Song, et al. · BMC Medical Genetics · 13

[Molecular and clinical study on homozygous or heterozygous large deletion of CYP21A2 gene in 21-OHD patients].

2019 · Y J Gao, B Q Yu, et al. · PubMed · 1

[Diagnostic value of multiplex ligation dependent probe amplification combined with Sanger sequencing in 21-hydroxylase deficiency].

2019 · Y J Gao, B Q Yu, et al. · PubMed · 1

Works count: 3

Citation count: 15

H-index: 1

I10-index: 1