Search of Somatic Mutations of NKX2-5 and GATA4 Genes in Chinese Patients with Sporadic Congenital Heart Disease

Early somatic mosaicism is a rare cause of long-QT syndrome

(2016) James Rush Priest et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Investigation of Somatic NKX2-5 Mutations in Chinese Children with Congenital Heart Disease

(2015) Jiayi Zheng et al.   International Journal of Medical Sciences

Lymphatic and Other Vascular Malformative/Overgrowth Disorders Are Caused by Somatic Mutations in PIK3CA

(2015) Valerie L. Luks et al.   JOURNAL OF PEDIATRICS

Recent advances in the study of somatic mosaicism and diseases other than cancer

(2014) Robert P Erickson   CURRENT OPINION IN GENETICS & DEVELOPMENT

Germline hereditary, somatic mutations and microRNAs targeting-SNPs in congenital heart defects

(2013) Saverio Sabina et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

Somatic mutations inNKX2-5,GATA4, andHAND1are not a common cause of tetralogy of Fallot or hypoplastic left heart

(2011) Giorgia Esposito et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects

(2011) Marleny Salazar et al.   European Journal of Medical Genetics

Birth Prevalence of Congenital Heart Disease Worldwide

(2011) Denise van der Linde et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Investigation of somatic NKX2-5, GATA4 and HAND1 mutations in patients with tetralogy of Fallot

(2011) Jian Wang et al.   PATHOLOGY

Paradigm of Genetic Mosaicism and Lone Atrial Fibrillation

(2010) Isabelle L. Thibodeau et al.   CIRCULATION

Genetic factors in non-syndromic congenital heart malformations

(2010) MW Wessels et al.   CLINICAL GENETICS

Somatic gene mutation and human disease other than cancer: An update

(2010) Robert P. Erickson   MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH

A functional genetic study identifies HAND1 mutations in septation defects of the human heart

(2009) Stella Marie Reamon-Buettner et al.   HUMAN MOLECULAR GENETICS