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المؤلفون: Xiaoyang Zhang, Hui Jing, Jinghao Zheng, Xiaomin He, Zhongqun Zhu, Qihua Fu, Huiwen Chen, Juan Geng, Zhaojing Zheng, Manchen Gao, Xiaoqing Zhang
المصدر: Pediatric Cardiology. 40:762-767
مصطلحات موضوعية: Heart Defects, Congenital, Heart Septal Defects, Ventricular, Male, China, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, DNA Copy Number Variations, endocrine system diseases, Locus (genetics), Heart defect, 030204 cardiovascular system & hematology, Gastroenterology, 03 medical and health sciences, 0302 clinical medicine, Asian People, Internal medicine, mental disorders, Prevalence, Humans, Medicine, In patient, Copy-number variation, Child, Likely pathogenic, business.industry, Infant, Newborn, Molecular pathogenesis, Infant, medicine.disease, Phenotype, 030228 respiratory system, Pulmonary Atresia, Child, Preschool, Pediatrics, Perinatology and Child Health, Cohort, Female, Cardiology and Cardiovascular Medicine, business, Pulmonary atresia, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31d2de49dfa78605cd2778a58a7f155dTest
https://doi.org/10.1007/s00246-019-02062-xTest -
2دورية أكاديمية
المؤلفون: Kai, Luo, Xiaoyang, Zhang, Jinghao, Zheng, Zhongqun, Zhu, Qi, Sun, Xiaomin, He, Zhiwei, Xu, Jinfen, Liu
المساهمون: National Key Research and Development Program of China
المصدر: Pediatric Cardiology ; volume 40, issue 5, page 965-972 ; ISSN 0172-0643 1432-1971