| Developing and validating noninvasive prenatal testing for de novo autosomal dominant monogenic diseases in Vietnam NY Nguyen, YT Lu, DA Nguyen, CC Nguyen, LT Dinh, MTT Tran, DC Tran, ... Personalized Medicine 20 (5), 425-433, 2023 | 1 | 2023 |
| The genetic landscape of chromosomal aberrations in 3776 Vietnamese fetuses with clinical anomalies during pregnancy DC Tran, MN Phan, HTT Dao, HDL Nguyen, DA Nguyen, QT Le, ... Personalized Medicine, 2024 | | 2024 |
| De novo variants of dominant monogenic disorders in Vietnam detected by a noninvasive prenatal test: a case series NT Tran, ST Vo, DA Nguyen, CC Nguyen, LT Dinh, MTT Tran, DC Tran, ... Personalized Medicine 20 (6), 467-475, 2023 | | 2023 |
| The genetic landscape of copy number variation in a Vietnamese cohort of 5008 fetuses with clinical anomalies during pregnancy DC Tran, HTT Dao, HDL Nguyen, DA Nguyen, QT Le, DTT Hoang, ... | | 2023 |
| EP24. 10: Prenatal diagnosis of hydrops fetalis secondary to lysosomal storage disease. ST Vo, HH Bui, H Giang, U Agarwal Ultrasound in Obstetrics & Gynecology 60, 2022 | | 2022 |
| EP25. 04: First trimester prenatal diagnosis of hypophosphatasia using ultrasound imaging and exome sequencing. ST Vo, MB Nguyen, HH Bui, H Giang, U Agarwal, NV Nguyen Ultrasound in Obstetrics & Gynecology 60, 2022 | | 2022 |
| EP27. 05: Prenatal diagnosis of fetal akinesia deformation sequence caused by RAPSN gene mutations: a case report. ST Vo, CV Ngo, CX Nguyen Ultrasound in Obstetrics & Gynecology 60, 2022 | | 2022 |
| VP16. 05: Prenatal diagnosis of Zellweger syndrome using clinical‐exome sequencing. ST Vo, TT Le, CX Nguyen, HX Tang, HT Nguyen, TN Nguyen, HH Bui, ... Ultrasound in Obstetrics & Gynecology 58, 2021 | | 2021 |
| VP16. 19: Prenatal diagnosis of a case of Noonan syndrome with RAF1 gene mutation using clinical‐exome sequencing ST Vo, TT Le, CX Nguyen, TN Tran Ultrasound in Obstetrics & Gynecology 58, 168-168, 2021 | | 2021 |
| VP47. 02: Prenatal diagnosis of primary microcephaly with novel compound heterozygous mutations of ASPM gene using clinical‐exome sequencing ST Vo, MH Pham, HH Bui, H Giang Ultrasound in Obstetrics & Gynecology 58, 299-299, 2021 | | 2021 |
| VP32. 04: Prenatal diagnosis a case of Jeune syndrome in combination with Down's syndrome ST Vo Ultrasound in Obstetrics & Gynecology 56, 189-189, 2020 | | 2020 |
| EP15. 02: Prenatal identification of novel compound heterozygous mutations associated with Ellis‐van Creveld syndrome: a case report. ST Vo, H Giang, NH Nguyen, TN Tran Ultrasound in Obstetrics & Gynecology 54, 2019 | | 2019 |
| EP17. 16: Case report: short rib polydactyly syndrome–type 2 (Majewski syndrome). ST Vo, TN Tran Ultrasound in Obstetrics & Gynecology 54, 2019 | | 2019 |
| Nghiên cứu các đặc điểm siêu âm và kết quả xử trí thai kỳ song thai một bánh nhau tại Bệnh viện Phụ sản Nhi Đà Nẵng HTT Di, VT Sơn Tạp chí Phụ sản 16 (4), 56-65, 2019 | | 2019 |
| Tiếp cận chẩn đoán trước sinh bất thường hệ xương thai nhi: nhân một trường hợp hội chứng Ellis-van Creveld VT Sơn, TN Thăng Tạp chí Phụ sản 16 (4), 139–142-139–142, 2019 | | 2019 |
| Hội chứng gương: báo cáo trường hợp và tổng quan tài liệu NV Hiền, VT Sơn Tạp chí Phụ sản 16 (2), 162–167-162–167, 2018 | | 2018 |
| Case of the Week# 596 TS Vo, MA El din Osman, C Jeanty | | |
| VAI TRÒ CỦA MẶT CẮT 3 MẠCH MÁU–KHÍ QUẢN TRONG CHẨN ĐOÁN BỆNH TIM BẨM SINH VT Sơn | | |
| Case of the Week# 554 TS Vo | | |
