Jia Liang

发表

MSX1 mutations and associated disease phenotypes: genotype-phenotype relations

Yijin Ren, Z. Bian, C. Carels, 2016, European Journal of Human Genetics.

Functional analysis of a novel missense mutation in AXIN2 associated with non-syndromic tooth agenesis.

Z. Bian, Jia Liang, Haitang Yue, 2016, European journal of oral sciences.

Two novel mutations in MSX1 causing oligodontia

Z. Bian, Jia Liang, Haitang Yue, 2020, PloS one.

A novel initiation codon mutation of PAX9 in a family with oligodontia.

Z. Bian, Chuanqi Qin, Jia Liang, 2016, Archives of oral biology.

Novel nonsense mutation in MSX1 causes tooth agenesis with cleft lip in a Chinese family.

Z. Bian, L. Meng, Dong Chen, 2012, European journal of oral sciences.

Novel missense mutations in PAX9 causing oligodontia.

Z. Bian, Guangtai Song, Qing Li, 2012, Archives of oral biology.

Mutation analysis in patients with nonsyndromic tooth agenesis using exome sequencing

Z. Bian, Guangtai Song, Jia Liang, 2022, Molecular genetics & genomic medicine.

Male inheritance of X-linked liver glycogenosis from an undiagnosed maternal grandfather in a Chinese pedigree: a report of two cases

Jia Liang, Yunqian Fang, Q. Lu, 2021 .

Novel missense mutations in PAX9 causing oligodontia.

Z. Bian, Guangtai Song, Qing Li, 2012, Archives of oral biology.