Tingting Zhang

发表

A novel mutation in NF1 gene of patient with Neurofibromatosis type 1: A case report and functional study

Wenli Lu, Zhiya Dong, Chuanyin Li, 2021, Molecular genetics & genomic medicine.

A novel intragenic microdeletion in RUNX 2 in a Chinese family with cleidocranial dysplasia

P. Gao, Y. Sun, Zhongli Zhang, 2016 .

Two different intragenic dystrophin deletions in a Chinese nuclear family with dystrophinopathies

Q. Fu, Kun Wang, Tingting Zhang, 2017 .

Clinical characteristics of a male child with non-classic lipoid congenital adrenal hyperplasia and literature review

L. Ye, Junqi Wang, Wenli Lu, 2022, Frontiers in Endocrinology.

Clinical and molecular characterization of thirty Chinese patients with congenital lipoid adrenal hyperplasia

G. Ning, L. Ye, Junqi Wang, 2020, The Journal of Steroid Biochemistry and Molecular Biology.

Characterization of Two Loss-of-Function NF1 Variants in Chinese Patients and Potential Molecular Interpretations of Phenotypes

Wenli Lu, Zhiya Dong, Chuanyin Li, 2021, Frontiers in Genetics.

Two loss‐of‐function ANKRD11 variants in Chinese patients with short stature and a possible molecular pathway

Yun Yang, Wenli Lu, Ji-hong Ni, 2020, American journal of medical genetics. Part A.

A novel PAX9 mutation found in a Chinese patient with hypodontia via whole exome sequencing.

Yanwei Sun, Jing Wu, Tingting Zhang, 2018, Oral diseases.

GALC mutations in Chinese patients with late-onset Krabbe disease: a case report

Tingting Zhang, Likun Chen, Shunzhi Zhuang, 2019, BMC Neurology.

A novel EDAR variant identified in non-syndromic tooth agenesis: Insights from molecular dynamics.

Tianqi Li, Tingting Zhang, Chonglv Feng, 2022, Archives of oral biology.

A Novel Loss-of-Function MKRN3 Variant in a Chinese Patient With Familial Precocious Puberty: A Case Report and Functional Study

Z. Tingting, Junqi Wang, Wenli Lu, 2021, Frontiers in Genetics.