Variety of prenatally diagnosed congenital heart disease in 22q11.2 deletion syndrome
Mi-Young Lee, Hye-Sung Won, Ju Won Baek, Jae-Hyun Cho, Jae-Yoon Shim, Pil-Ryang Lee, Ahm Kim
Obstet Gynecol Sci. 2014;57(1):11-16.   Published online 2014 Jan 16     DOI:
Citations to this article as recorded by Crossref logo
Prevalence of associated extracardiac anomalies in prenatally diagnosed congenital heart diseases
Chi-Son Chang, Sir-yeon Hong, Seo-yeon Kim, Yoo-min Kim, Ji-Hee Sung, Suk-Joo Choi, Soo-young Oh, Cheong-Rae Roh, Jinyoung Song, June Huh, I-Seok Kang, David Scott Winlaw
PLOS ONE.2021; 16(3): e0248894.     CrossRef
22q11.2 deletion syndrome and congenital heart disease
Elizabeth Goldmuntz
American Journal of Medical Genetics Part C: Seminars in Medical Genetics.2020; 184(1): 64.     CrossRef
Prenatal screening of DiGeorge (22q11.2 deletion) syndrome by abnormalities of the great arteries among Thai pregnant women
Kuntharee Traisrisilp, Fuanglada Tongprasert, Kasemsri Srisupundit, Suchaya Luewan, Theera Tongsong
Obstetrics & Gynecology Science.2020; 63(3): 330.     CrossRef
Duplication and Deletion of 22q11 Associated with Anomalous Pulmonary Venous Connection
Ruixue Cao, Sijie Liu, Chunjie Liu, Sun Chen, Fen Li, Kun Sun, Rang Xu
Pediatric Cardiology.2018; 39(3): 585.     CrossRef
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers
Marta Unolt, Paolo Versacci, Silvia Anaclerio, Caterina Lambiase, Giulio Calcagni, Matteo Trezzi, Adriano Carotti, Terrence Blaine Crowley, Elaine H. Zackai, Elizabeth Goldmuntz, James William Gaynor, Maria Cristina Digilio, Donna M. McDonald-McGinn, Brun
American Journal of Medical Genetics Part A.2018; 176(10): 2087.     CrossRef
CNNdel: Calling Structural Variations on Low Coverage Data Based on Convolutional Neural Networks
Jing Wang, Cheng Ling, Jingyang Gao
BioMed Research International.2017; 2017: 1.     CrossRef
The benefits and limitations of cell-free DNA screening for 22q11.2 deletion syndrome
Lorraine Dugoff, Michael T. Mennuti, Donna M. McDonald-McGinn
Prenatal Diagnosis.2017; 37(1): 53.     CrossRef
Targeted capture enrichment assay for non-invasive prenatal testing of large and small size sub-chromosomal deletions and duplications
Maria C. Neofytou, Kyriakos Tsangaras, Elena Kypri, Charalambos Loizides, Marios Ioannides, Achilleas Achilleos, Petros Mina, Anna Keravnou, Carolina Sismani, George Koumbaris, Philippos C. Patsalis, Noam Shomron
PLOS ONE.2017; 12(2): e0171319.     CrossRef
Machine-learning-aided precise prediction of deletions with next-generation sequencing
Rui Guan, Jing-yang Gao
Journal of Central South University.2016; 23(12): 3239.     CrossRef
Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion
Yen-Ni Chen, Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Pei-Chen Wu, Tung-Yao Chang, Peih-Shan Wu, Chien-Wen Yang, Wayseen Wang
Taiwanese Journal of Obstetrics and Gynecology.2016; 55(1): 117.     CrossRef
Screening ultrasonography in pregnancy
Ba-Da Jeong, Hye-Sung Won
Journal of the Korean Medical Association.2015; 58(11): 1003.     CrossRef
Current Status of Testing for Microdeletion Syndromes and Rare Autosomal Trisomies Using Cell-Free DNA Technology
Yuval Yaron, Jacques Jani, Maximilian Schmid, Dick Oepkes
Obstetrics & Gynecology.2015; 126(5): 1095.     CrossRef