Suchergebnisse - "Ni, Fenfen"

PubPharm (3)

1

A genomic association study revealing subphenotypes of childhood steroid-sensitive nephrotic syndrome in a larger genomic sequencing cohort

enthalten in: Genes & diseases | 2024

von Chan, H. | Ni, F. | Zhao, B. | +20

2

Whole-exome sequencing of a multicenter cohort identifies genetic changes associated with clinical phenotypes in pediatric nephrotic syndrome

enthalten in: Genes & diseases | 2022

von Jiao, J. | Wang, L. | Ni, F. | +22

3

Clinical feature and variant analysis of a case with hereditary hypophosphatemic rickets with hypercalciuria

enthalten in: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020

von Liu, L. | Gao, X. | Ma, Y. | +3

1
[1]