J. Zhang

发表

First Mal de Meleda report in Chinese Mainland: two families with a recurrent homozygous missense mutation in SLURP‐1

Z. Yao, R. Cheng, M. Li, 2016, Journal of the European Academy of Dermatology and Venereology : JEADV.

Palmoplantar keratoderma: a new phenotype in patients with hypotrichosis resulted from lanosterol synthase gene mutations

X. Y. Wang, J. Han, Y. Wang, 2022, Journal of the European Academy of Dermatology and Venereology : JEADV.

Phenotypic analysis of atopic dermatitis in children aged 1–12 months: elaboration of novel diagnostic criteria for infants in China and estimation of prevalence

Hong Wang, T. Bieber, Y. Luo, 2019, Journal of the European Academy of Dermatology and Venereology : JEADV.

Mutations in the mevalonate pathway genes in Chinese patients with porokeratosis

N. Wilson, F. Chen, X. Li, 2016, Journal of the European Academy of Dermatology and Venereology : JEADV.

Comprehensive molecular characterization of renal cell carcinoma in the Chinese population

W. Kong, M. Li, F. Lou, 2021, European Urology.

Guidelines for management of androgenetic alopecia based on BASP classification–the Asian consensus committee guideline

G. Choi, M. Zheng, S. Chow, 2013, Journal of the European Academy of Dermatology and Venereology : JEADV.

Updated review of genetic reticulate pigmentary disorders

Maolan Li, Z. Yao, M. Li, 2017, The British journal of dermatology.

CHILD syndrome mimicking verrucous nevus in a Chinese patient responded well to the topical therapy of compound of simvastatin and cholesterol

Y. Gu, Z. Yao, X. Yu, 2018, Journal of the European Academy of Dermatology and Venereology : JEADV.

Café au lait macules overlying segmental macular hyperpigmentation in a paediatric patient: an early sign for mosaic neurofibromatosis type 1

Z. Yao, M. Li, W. Qin, 2020, The British journal of dermatology.

Report of a child with sporadic familial progressive hyper‐ and hypopigmentation caused by a novel KITLG mutation

Z. Yao, R. Cheng, M. Li, 2016, The British journal of dermatology.

Exome sequencing identifies a TCF4 mutation in a Chinese pedigree with symmetrical acral keratoderma

K. Zeng, P. Chen, S. Sun, 2018, Journal of the European Academy of Dermatology and Venereology : JEADV.

Lentiginous phenotypes caused by diverse pathogenic genes (SASH1 and PTPN11): clinical and molecular discrimination

Z. Yao, R. Cheng, M. Li, 2016, Clinical genetics.

A rare RECQL4 indel mutation in a Chinese patient with Rothmund–Thomson syndrome

Z. Yao, R. Cheng, Jia Zhang, 2015, Journal of the European Academy of Dermatology and Venereology : JEADV.

Genotype–phenotype correlation of xeroderma pigmentosum in a Chinese Han population

Z. Yao, R. Cheng, M. Li, 2015, The British journal of dermatology.