Suchergebnisse - "Asian Continental Ancestry Group"

PubPharm (18)

1

Mutation scanning of the COQ2 gene in ethnic Chinese patients with multiple-system atrophy

enthalten in: Neurobiology of aging | 2015

von Chen, Y. | Zhao, B. | Cao, B. | +6

2

VCP gene analyses in Japanese patients with sporadic amyotrophic lateral sclerosis identify a new mutation

enthalten in: Neurobiology of aging | 2015

von Hirano, M. | Nakamura, Y. | Saigoh, K. | +5

3

Identification of PSEN1 mutations p.M233L and p.R352C in Han Chinese families with early-onset familial Alzheimer's disease

enthalten in: Neurobiology of aging | 2015

von Jiang, H. | Li, G. | Dai, S. | +7

4

Government-funded universal newborn hearing screening and genetic analyses of deafness predisposing genes in Taiwan

enthalten in: International journal of pediatric otorhinolaryngology | 2015

von Chu, C. | Chen, Y. | Lee, Y. | +3

5

Genetic counseling for a three-generation Chinese family with Waardenburg syndrome type II associated with a rare SOX10 mutation

enthalten in: International journal of pediatric otorhinolaryngology | 2015

von Chen, K. | Zong, L. | Zhan, Y. | +3

6

Identification of a new non‐synonymous mutation in HLA‐B gene, HLA‐B15:320, in a Chinese individual by sequence‐based typing

enthalten in: Tissue antigens | 2015

von Dai, D. | Zhou, X. | Cai, J.

7

A gain-of-function mutation in TRPV3 causes focal palmoplantar keratoderma in a Chinese family

enthalten in: The journal of investigative dermatology | 2015

von He, Y. | Zeng, K. | Zhang, X. | +16

8

Genetic heterogeneity of pseudoxanthoma elasticum: the Chinese signature profile of ABCC6 and ENPP1 mutations

enthalten in: The journal of investigative dermatology | 2015

von Jin, L. | Jiang, Q. | Wu, Z. | +5

9

Next generation sequencing as a rapid molecular diagnosis for Marfan syndrome in a Chinese family with mutations in the fibrillin-1 gene

enthalten in: Clinica chimica acta | 2015

von Xiao, Y. | Liu, Y. | Yang, K. | +6

10

High resolution melting analytical platform for rapid prenatal and postnatal diagnosis of β-thalassemia common among Southeast Asian population

enthalten in: Clinica chimica acta | 2015

von Prajantasen, T. | Fucharoen, S. | Fucharoen, G.