Suchergebnisse - "Wu, Bing-Bing"

PubPharm (35)

1

Relationship between phenotype and genotype of 102 Chinese newborns with Prader-Willi syndrome

enthalten in: Molecular biology reports | 2019

von Ge, M. | Gao, Y. | Wu, B. | +5

2

Expanding the spectrum of A20 haploinsufficiency in two Chinese families : cases report

enthalten in: BMC medical genetics | 2019

von Li, G. | Liu, H. | Guan, W. | +3

3

Expanding the spectrum of A20 haploinsufficiency in two Chinese families: cases report

enthalten in: BMC medical genetics | 2019

von Li, G. | Liu, H. | Guan, W. | +3

4

Expanding the spectrum of A20 haploinsufficiency in two Chinese families: cases report

enthalten in: BMC medical genetics | 2019

von Li, G. | Liu, H. | Guan, W. | +3

5

Relationship between phenotype and genotype of 102 Chinese newborns with Prader–Willi syndrome

enthalten in: Molecular biology reports | 2019

von Ge, M. | Gao, Y. | Wu, B. | +5

6

Relationship between phenotype and genotype of 102 Chinese newborns with Prader–Willi syndrome

enthalten in: Molecular biology reports | 2019

von Ge, M. | Gao, Y. | Wu, B. | +5

7

Relationship between phenotype and genotype of 102 Chinese newborns with Prader–Willi syndrome

enthalten in: Molecular biology reports | 2019

von Ge, M. | Gao, Y. | Wu, B. | +5

8

Dissecting cell diversity and connectivity in skeletal muscle for myogenesis

enthalten in: Cell death & disease | 2019

von Liu, Y. | Wu, B. | Gong, L. | +11

9

A mutation in PIK3CD gene causing pediatric systemic lupus erythematosus : A case report

enthalten in: Medicine | 2019

von Li, G. | Liu, H. | Guan, W. | +4

10

Role of PUF60 gene in Verheij syndrome : a case report of the first Chinese Han patient with a de novo pathogenic variant and review of the literature

enthalten in: BMC medical genomics | 2018

von Xu, Q. | Li, C. | Wang, Y. | +4