Suchergebnisse - "Liu, Yalan"

PubPharm (4)

1

A novel ABHD12 nonsense variant in Usher syndrome type 3 family with genotype-phenotype spectrum review

enthalten in: Gene | 2019

von Li, T. | Feng, Y. | Liu, Y. | +15

2

Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I

enthalten in: Gene | 2018

von Niu, Z. | Li, J. | Tang, F. | +9

3

Disruption of Contactin 4 in two subjects with autism in Chinese population

enthalten in: Gene | 2012

von Guo, H. | Xun, G. | Peng, Y. | +12

4

Disruption of Contactin 4 in two subjects with autism in Chinese population

enthalten in: Gene | 2012

von Guo, H. | Xun, G. | Peng, Y. | +12

1
[1]