Suchergebnisse - "Shiyue Mei"

PubPharm (14)

1

Impact of COVID-19 on the Epidemiological Features of Mycoplasma pneumoniae Infection in Children with Community-Acquired Pneumonia in Henan, China

in: Microbiology Spectrum | 2023

von Lifeng Li | Pengbo Guo | Jiayue Ma | +2

2

Clinical and genetic analysis of two patients with primary ciliary dyskinesia caused by a novel variant of DNAAF2

in: BMC Pediatrics | 2023

von Lili Dong | Lei Zhang | Xiao Li | +6

3

Influence of COVID-19 pandemic on the epidemiology of Mycoplasma pneumoniae infections among hospitalized children in Henan, China

in: Heliyon | 2023

von Jiayue Ma | Pengbo Guo | Shiyue Mei | +6

4

Genetic and Phenotype Analysis of a Chinese Cohort of Infants and Children With Epilepsy

enthalten in: Frontiers in genetics | 2022

von Chuan, Z. | Ruikun, C. | Qian, L. | +14

5

HPDL mutations identified by exome sequencing are associated with infant neurodevelopmental disorders

in: Molecular Genetics & Genomic Medicine | 2022

von Yanhong Wang | Xuan Zheng | Chao Feng | +5

6

Expansion of the mutation spectrum and phenotype of USP7-related neurodevelopmental disorder

in: Frontiers in Molecular Neuroscience | 2022

von Hong Zheng | Hong Zheng | Shiyue Mei | +9

7

A novel variant in UBE3A in a family with multigenerational intellectual disability and developmental delay

in: Molecular Genetics & Genomic Medicine | 2022

von Xuechao Zhao | Yuting Zheng | Li Wang | +3

8

Exons deletion of CNKSR2 gene identified in X-linked syndromic intellectual disability

enthalten in: BMC medical genetics | 2020

von Daoqi, M. | Guohong, C. | Yuan, W. | +3

9

Exons deletion of CNKSR2 gene identified in X-linked syndromic intellectual disability

enthalten in: BMC medical genetics | 2020

von Daoqi, M. | Guohong, C. | Yuan, W. | +3

10

Exons deletion of CNKSR2 gene identified in X-linked syndromic intellectual disability

enthalten in: BMC medical genetics | 2020

von Daoqi, M. | Guohong, C. | Yuan, W. | +3