Last Posted: Feb 14, 2019
- Actions in Support of Newborn Screening for Critical Congenital Heart Disease - United States, 2011-2018.
Glidewell Jill et al. MMWR. Morbidity and mortality weekly report 2019 Feb 68(5) 107-111 - Actions in Support of Newborn Screening for Critical Congenital Heart Disease United States, 20112018
CDC MMWR, February 7, 2019 - Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Lord Jenny et al. Lancet (London, England) 2019 Jan - Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.
Pierpont Mary Ella et al. Circulation 2018 Nov 138(21) e653-e711 - Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome.
Cai Meiying et al. Medicine 2018 Dec 97(50) e13617 - Prevalence of Noonan spectrum disorders in a pediatric population with valvar pulmonary stenosis.
Anderson Kailyn et al. Congenital heart disease 2018 Dec - Identification of clinically actionable variants from genome sequencing of families with congenital heart disease.
Alankarage Dimuthu et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Oct - Genetic evaluation of patients with congenital heart disease.
Geddes Gabrielle C et al. Current opinion in pediatrics 2018 Aug - Genetic Testing and Pregnancy Outcome Analysis of 362 Fetuses with Congenital Heart Disease Identified by Prenatal Ultrasound.
Luo Shiyu et al. Arquivos brasileiros de cardiologia 2018 Aug - Targeted Next-Generation Sequencing in Patients with Non-syndromic Congenital Heart Disease.
Pulignani Silvia et al. Pediatric cardiology 2018 Apr 39(4) 682-689
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