Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Nhat Thang Tran"'
Autor:
Phuoc-Loc Doan, Duy-Anh Nguyen, Quang Thanh Le, Diem-Tuyet Thi Hoang, Huu Du Nguyen, Canh Chuong Nguyen, Kim Phuong Thi Doan, Nhat Thang Tran, Thi Minh Thi Ha, Thu Huong Nhat Trinh, Van Thong Nguyen, Chi Thuong Bui, Ngoc-Diep Thi Lai, Thanh Hien Duong, Hai-Ly Mai, Pham-Uyen Vinh Huynh, Thu Thanh Thi Huynh, Quang Vinh Le, Thanh Binh Vo, Thi Hong-Thuy Dao, Phuong Anh Vo, Duy-Khang Nguyen Le, Ngoc Nhu Thi Tran, Quynh Nhu Thi Tran, Yen-Linh Thi Van, Huyen-Trang Thi Tran, Hoai Thi Nguyen, Phuong-Uyen Nguyen, Thanh-Thuy Thi Do, Dinh-Kiet Truong, Hung Sang Tang, Ngoc-Phuong Thi Cao, Tuan-Thanh Lam, Le Son Tran, Hoai-Nghia Nguyen, Hoa Giang, Minh-Duy Phan
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract α-Thalassemia is a common inherited blood disorder manifested mainly by the deletions of α-globin genes. In geographical areas with high carrier frequencies, screening of α-thalassemia carrier state is therefore of vital importance. This
Externí odkaz:
https://doaj.org/article/4033a621471f4d4bb98af70be98bf7bc
Autor:
Tat‐Thanh Nguyen, Quang‐Thanh Le, Diem‐Tuyet Thi Hoang, Huu Du Nguyen, Thi Minh Thi Ha, My‐Nhi Ba Nguyen, Thanh‐Thuy Thi Ta, Nhat Thang Tran, Thu Huong Nhat Trinh, Kim Phuong Thi Doan, Duc Tam Lam, Son Tra Thi Tran, Thanh Xuan Nguyen, Hong‐Thinh Le, Van Tuan Ha, Manh Hoan Nguyen, Ba‐Liem Kim Le, My Linh Duong, Trung Ha Pham, Anh Tuan Tran, Xuan Lan Thi Phan, Thanh Liem Huynh, Lan‐Phuong Thi Nguyen, Thanh Binh Vo, Duy‐Khang Nguyen Le, Ngoc Nhu Thi Tran, Quynh Nhu Thi Tran, Yen‐Linh Thi Van, Bich‐Ngoc Thi Huynh, Thanh‐Phương Thi Nguyen, Trang Thi Dao, Lan Phuong Thi Nguyen, Truong‐Giang Vo, Thanh‐Thuy Thi Do, Dinh‐Kiet Truong, Hung Sang Tang, Minh‐Duy Phan, Hoai‐Nghia Nguyen, Hoa Giang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 7, Pp n/a-n/a (2022)
Abstract Background Several inherited metabolic diseases are underreported in Vietnam, namely glucose‐6‐phosphate dehydrogenase deficiency (G6PDd), phenylketonuria (PKU) and galactosemia (GAL). Whilst massively parallel sequencing (MPS) allows re
Externí odkaz:
https://doaj.org/article/037b4a2351ac4123ba7b778f1ae0fea6
Autor:
Hai Xuan Tang, Y‐Thanh Lu, Thi Minh Thi Ha, Nhat‐Thang Tran, Doan Minh Dang, Son Xuan Ly, Thu Ha Thi Bui, Son Ta Vo, Minh Doan Thai, Vu Dinh Nguyen, Thong Van Nguyen, Linh Thuy Dinh, Lan‐Anh Thi Luong, Kim‐Phuong Doan, Kim Huong Thi Nguyen, Thanh‐Thuy Thi Do, Dinh‐Kiet Truong, Hoa Giang, Hoai‐Nghia Nguyen, Thu Huong Nhut Trinh, Hung Sang Tang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 6, Pp n/a-n/a (2024)
Abstract Background De novo variations are a primary cause of Rett syndrome and Tubulinopathy, accounting for over 90% of cases. Some studies have identified and documented parental inheritance by mosaicism in these two disorders, albeit with limited
Externí odkaz:
https://doaj.org/article/19102d2952084acf94b9f1f48e3f6b86
Autor:
Danh-Cuong Tran, Hong-Thuy Thi Dao, Hong-Dang Luu Nguyen, Duy-Anh Nguyen, Quang Thanh Le, Diem-Tuyet Thi Hoang, Nhat Thang Tran, Thi Minh Thi Ha, Thuy Linh Dinh, Canh Chuong Nguyen, Kim Phuong Thi Doan, Lan Anh Thi Luong, Ta Son Vo, Thu Huong Nhat Trinh, Van Thong Nguyen, Phuong-Anh Ngoc Vo, Yen-Nhi Nguyen, My-An Dinh, Minh Ngoc Phan, Phuoc-Loc Doan, Thanh-Thuy Thi Do, Quynh-Tho Thi Nguyen, Dinh-Kiet Truong, Hoai-Nghia Nguyen, Minh-Duy Phan, Hung-Sang Tang, Hoa Giang
Copy number variation (CNV) analysis is a powerful tool for discovering structural genomic variation. Still, no program uses this tool to analyze chromosomal aneuploidies in the Vietnamese population. Pregnant women attending routine prenatal checkup
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fcb57f2891efecb7b3b9cc563d2e66b
https://doi.org/10.21203/rs.3.rs-2410361/v1
https://doi.org/10.21203/rs.3.rs-2410361/v1
Autor:
Tuan-Thanh Lam, Doan-Tu Nguyen, Quang Thanh Le, Duy-Anh Nguyen, Diem-Tuyet Thi Hoang, Huu Du Nguyen, Canh Chuong Nguyen, Kim Phuong Thi Doan, Nhat-Thang Tran, Thi Minh Thi Ha, Thu Huong Nhat Trinh, Van Thong Nguyen, Duc Tam Lam, Minh Tam Le, Xuan Thao Nguyen, Thu-Hang Thi Ho, Trung Hoanh Tran, Viet Thang Ho, Thanh Van Bui, Van Trong Nguyen, Phuoc Ba Hoang, Hoai Thanh Nguyen, Manh Hoan Nguyen, Thanh-Binh Vo, Duy-Khang Nguyen Le, Thao Ngoc Truong, Hong-Thuy Thi Dao, Phuong-Anh Ngoc Vo, Thien-Chi Van Nguyen, Ngoc-Nhu Thi Tran, Quynh-Nhu Thi Tran, Yen-Linh Thi Van, Thanh-Thanh Thi Nguyen, Bich-Ngoc Thi Huynh, Thanh-Phuong Thi Nguyen, Kim-Van Thi Tran, Cong-Trai Nguyen, Phuoc-Loc Doan, Thanh-Dat Nguyen, Thanh-Thuy Thi Do, Dinh-Kiet Truong, Hung Sang Tang, Ngoc-Phuong Thi Cao, Minh-Duy Phan, Hoa Giang, Hoai-Nghia Nguyen
Publikováno v:
Hemoglobin. 46(4)
Vietnam has a high thalassemia burden. We collected blood samples from 5880 pregnant Vietnamese women during prenatal health checks to assess thalassemia carrier frequency using combined gap-polymerase chain reaction (gap-PCR) and targeted next-gener
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6efdb8cb432fe9844a0dbcd698a4c87
https://pubmed.ncbi.nlm.nih.gov/35993587
https://pubmed.ncbi.nlm.nih.gov/35993587
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Yen Linh Thi Van, Thanh Thuy Thi Do, Van T. M. Nguyen, Vu Uyen Tran, Minh-Duy Phan, Huu Nguyen Nguyen, Thi Hong Thuy Dao, Nhat Thang Tran, Hoai-Nghia Nguyen, Hong Anh Thi Pham, Nien Vinh Lam, Quynh Tho Thi Nguyen, Dinh Kiet Truong, Thu Huong Nhat Trinh, Ngoc Mai Nguyen, Phuong Cao Thi Ngoc, Thanh Binh Vo, Hoang Giang Vu, Phuong Anh Ngoc Vo, Quynh Tram Nguyen Bui, Hoa Giang, Ngoc Hieu Tran
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-8 (2020)
Scientific Reports
Scientific Reports
The under-representation of several ethnic groups in existing genetic databases and studies have undermined our understanding of the genetic variations and associated traits or diseases in many populations. Cost and technology limitations remain the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a86e3c256f8707bd5b3aa982526b8cd5
http://link.springer.com/article/10.1038/s41598-020-76245-5
http://link.springer.com/article/10.1038/s41598-020-76245-5
Publikováno v:
Tạp chí Phụ sản. 18:32-37
Mục tiêu nghiên cứu: Mô tả kết cục thai kỳ các trường hợp thai nhỏ so với tuổi thai được chẩn đoán từ 28 đến 36 tuần tại Bệnh viện Phụ sản Thành phố Cần Thơ và khảo sát các yếu tố li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea77d4cc3cf5b305bc278f61fb4a701f
https://doi.org/10.46755/vjog.2020.1.771
https://doi.org/10.46755/vjog.2020.1.771
Autor:
Danh Cuong Tran, Thanh-Thanh Thi Nguyen, Ngoc-Lan Thi Hoang, Lan-Anh Thi Luong, Kim-Phuong Thi Doan, Minh Thi Thi Ha, Nhat-Thang Tran, Van-Thong Nguyen, Thu-Huong Nhat Trinh, Ngoc-Trinh Kieu Nguyen, Cong-Trai Nguyen, Thanh-Dat Nguyen, xQuynh-Tho Thi Nguyen, Thanh-Thuy Thi Do, Dinh-Kiet Truong, Hoa Giang, Hoai-Nghia Nguyen, Hung-Sang Tang, Minh-Duy Phan
To demonstrate the prevalence of maternal mosaic monosomy X (MMXO) in a cohort of pregnant women in Vietnam. All 105,594 singleton pregnant women undergoing noninvasive prenatal screening (NIPS) between January 2019 and February 2021 in Vietnam were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3344b238b5e8933e4e4e4e3fe8c96ce7
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.