Prenatal molecular diagnosis in hypertrophic cardiomyopathy: report of the first case-Reference-Cited by-同舟云学术

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Prenatal molecular diagnosis in hypertrophic cardiomyopathy: report of the first case

Published:2004-09 Issue:9 Volume:24 Page:701-703
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Charron Philippe,Héron Delphine,Gargiulo Marcela,Feingold Josué,Oury Jean-François,Richard Pascale,Komajda Michel

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Cited by 27 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Cryo-EM structure of the folded-back state of human β-cardiac myosin*;2023-04-18

2. Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association;Circulation: Genomic and Precision Medicine;2021-10

3. 2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families;Journal of Arrhythmia;2021-04-08

4. 2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families;Heart Rhythm;2021-01

5. Ultrasound and genetic detection of fetal hypertrophic cardiomyopathy in second trimester of pregnancy;BMJ Case Reports;2021-01

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