Detalhe da pesquisa
1.
Importance of genetic testing in unexplained cardiac arrest.
Eur Heart J
; 43(32): 3071-3081, 2022 08 21.
Artigo
Inglês
| MEDLINE | ID: mdl-35352813
2.
Missense variants in the spectrin repeat domain of DSP are associated with arrhythmogenic cardiomyopathy: A family report and systematic review.
Am J Med Genet A
; 182(10): 2359-2368, 2020 10.
Artigo
Inglês
| MEDLINE | ID: mdl-32808748
3.
Deep Learning-Augmented ECG Analysis for Screening and Genotype Prediction of Congenital Long QT Syndrome.
JAMA Cardiol
; 9(4): 377-384, 2024 Apr 01.
Artigo
Inglês
| MEDLINE | ID: mdl-38446445
4.
Diagnostic and Therapeutic Misconception: Parental Expectations and Perspectives Regarding Genetic Testing for Developmental Disorders.
J Autism Dev Disord
; 49(1): 363-375, 2019 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-30284667
5.
Novel Gain-of-Function Variant in CACNA1C Associated With Timothy Syndrome, Multiple Accessory Pathways, and Noncompaction Cardiomyopathy.
Circ Genom Precis Med
; 13(6): e003123, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-33191761