Detalhe da pesquisa
1.
Perceived knowledge, attitudes and practices regarding the medical consortium among medical staff in Sichuan, China: a cross-sectional survey.
BMC Health Serv Res
; 23(1): 1318, 2023 Nov 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38031073
2.
Correction: High-resolution DNA size enrichment using a magnetic nano-platform and application in non-invasive prenatal testing.
Analyst
; 147(3): 542, 2022 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-34989362
3.
G3viz: an R package to interactively visualize genetic mutation data using a lollipop-diagram.
Bioinformatics
; 36(3): 928-929, 2020 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31393560
4.
High-resolution DNA size enrichment using a magnetic nano-platform and application in non-invasive prenatal testing.
Analyst
; 145(17): 5733-5739, 2020 Aug 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-32748914
5.
The health service capacity of primary health care in West China: different perspectives of physicians and their patients.
BMC Health Serv Res
; 19(1): 143, 2019 Feb 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-30819168
6.
Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions.
Genet Med
; 17(7): 578-86, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25356970
7.
ELP2 is a novel gene implicated in neurodevelopmental disabilities.
Am J Med Genet A
; 167(6): 1391-5, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25847581
8.
New Insights into the Genetics of Fetal Megacystis: ACTG2 Mutations, Encoding γ-2 Smooth Muscle Actin in Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (Berdon Syndrome).
Fetal Diagn Ther
; 38(4): 296-306, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25998219
9.
Expanding the clinical and mutational spectrum of Kaufman oculocerebrofacial syndrome with biallelic UBE3B mutations.
Hum Genet
; 133(7): 939-49, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24615390
10.
Advancements in the ERK1/2 Signaling Pathway Affecting Male Reproduction.
Front Biosci (Landmark Ed)
; 29(1): 23, 2024 01 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38287801
11.
Fatigue of an Aluminum Foam Sandwich Formed by Powder Metallurgy.
Materials (Basel)
; 16(3)2023 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-36770231
12.
Multi-functional Strategy: Ammonium Citrate-Modified SnO2 ETL for Efficient and Stable Perovskite Solar Cells.
ACS Appl Mater Interfaces
; 14(38): 43975-43986, 2022 Sep 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36103625
13.
The Contributing Factors of Delayed-Onset Post-traumatic Stress Disorder Symptoms: A Nested Case-Control Study Conducted After the 2008 Wenchuan Earthquake.
Front Public Health
; 9: 682714, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35004555
14.
Risk factors of post-traumatic stress disorder 10 years after Wenchuan earthquake: a population-based case-control study.
Epidemiol Psychiatr Sci
; 30: e25, 2021 Mar 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33729117
15.
Prevalence and Influencing Factors of Post-Traumatic Stress Disorder Among Survivors in the Hard-Hit Areas Ten Years After the Wenchuan Earthquake: A Cross-Sectional Study.
Neuropsychiatr Dis Treat
; 16: 933-941, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32308397
16.
Neurexin 1alpha structural variants associated with autism.
Neurosci Lett
; 438(3): 368-70, 2008 Jun 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-18490107
17.
Genetic analysis of the GRIK2 modifier effect in Huntington's disease.
BMC Neurosci
; 7: 62, 2006 Sep 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-16959037
18.
Diagnostic Exome Sequencing and Tailored Bioinformatics of the Parents of a Deceased Child with Cobalamin Deficiency Suggests Digenic Inheritance of the MTR and LMBRD1 Genes.
JIMD Rep
; 15: 29-37, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-24664876
19.
Congenital lethal motor neuron disease with a novel defect in ribosome biogenesis.
Neurology
; 82(15): 1322-30, 2014 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24647030
20.
A human de novo mutation in MYH10 phenocopies the loss of function mutation in mice.
Rare Dis
; 1: e26144, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-25003005