Search Results - Van Khanh Tran

Rapid method for targeted prenatal diagnosis of Duchenne muscular dystrophy in Vietnam by Minh-Hieu Ta, Thinh Huy Tran, Ngoc-Hai Do, Le Anh-Tuan Pham, The-Hung Bui, Van-Thanh Ta, Van-Khanh Tran

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Dentinogenesis Imperfecta and Caries in Osteogenesis Imperfecta among Vietnamese Children by Huong Thi Thu Nguyen, Dung Chi Vu, Duc Minh Nguyen, Quang Dinh Dang, Van Khanh Tran, Hung Le, Son Minh Tong

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A novel IGHMBP2 variant and clinical diversity in Vietnamese SMARD1 and CMT2S patients by Van Khanh Tran, Van Khanh Tran, My Ha Cao, Thi Thanh Hai Nguyen, Phuong Thi Le, Hai Anh Tran, Dung Chi Vu, Ha Thu Nguyen, Mai Thi Phương Nguyen, The-Hung Bui, The-Hung Bui, Thanh Binh Nguyen, Thanh Van Ta, Thanh Van Ta, Thinh Huy Tran, Thinh Huy Tran

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Whole exome sequencing analysis in a couple with three children who died prematurely due to carnitine-acylcarnitine translocase deficiency by Van Khanh Tran, Quang Minh Diep, Zilong Qiu, Thi Phuong Le, Long Duy Do, Hai Anh Tran, The-Hung Bui, Thanh Van Ta, Thinh Huy Tran

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Micronutrient deficiencies and the double burden of malnutrition in Vietnamese female adolescents: a national cross-sectional study in 2020Research in context by Xiaomian Tan, Pui Yee Tan, Somphos Vicheth Som, Son Duy Nguyen, Do Thanh Tran, Nga Thuy Tran, Van Khanh Tran, J. Bernadette Moore, Yun Yun Gong

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Microcephaly primary hereditary (MCPH): Report of novel ASPM variants and prenatal diagnosis in a Vietnamese family by Thinh Huy Tran, Quang Minh Diep, My Ha Cao, Long Hoang Luong, Van Anh Pham, Oanh Thi Lan Dinh, The-Hung Bui, Thanh Van Ta, Van Khanh Tran

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Prenatal diagnosis of a case with SEA-HPFH deletion thalassemia with whole HBB gene deletion by Ha Ly Thi Thanh, Huong Le Thi Thanh, Long Hoang Luong, Thinh Huy Tran, Su-Ching Liu, Hai Nam Truong, Thanh Van Ta, The - Hung Bui, Van Khanh Tran

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Mosaicism in carrier of Duchenne muscular dystrophy mutation - Implication for prenatal diagnosis by Linh Thuy Dinh, Duc Hinh Nguyen, Long Hoang Luong, Phuong Thi Le, Tuan Pham Le-Anh, Dat Quoc Tran, Thinh Huy Tran, The-Hung Bui, Thanh Van Ta, Van Khanh Tran

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Assessment of 6 STR loci for prenatal diagnosis of Duchenne Muscular Dystrophy by Linh Thuy Dinh, Van Khanh Tran, Long Hoang Luong, Phuong Thi Le, Anh Duy Nguyen, Bang Suong Thi Nguyen, Dung Vu Chi, Thinh Huy Tran, The-Hung Bui, Thanh Van Ta, Duc Hinh Nguyen

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Preimplantation genetic testing (PGT) for hemophilia A: Experience from one center by Thi Minh Phuong Bui, Van Khanh Tran, Thi Thanh Hai Nguyen, Thi Phuong Le, Thi Mai Nguyen, Hai Anh Tran, Vu Dung Luu, Manh Ha Nguyen, The-Hung Bui, Thanh Van Ta, Thinh Huy Tran

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Application of short tandem repeats (STRs) in the preimplantation genetic diagnosis (PGD) of α-thalassemia by Vu Viet Ha Vuong, Phuoc-Dung Nguyen, Nha Nguyen Thi, Phuong Le Thi, Dang Thi Minh Nguyet, Manh Ha Nguyen, Hai Anh Tran, Nhat-Min, The-Hung Bui, Thinh Huy Tran, Thanh Van Ta, Van-Khanh Tran

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Triple burden of malnutrition among Vietnamese 0·5-11-year-old children in 2020-2021: results of SEANUTS II Vietnam by Nga Thuy Tran, Van Khanh Tran, Duong Thanh Tran, Tu Tran Ngoc Nguyen, Son Duy Nguyen, Ha Thu Nguyen, Tu Song Nguyen, Tung Van Thanh Le, Phuong Thi Lan Nguyen, Hanh Thi Dang, Hoa Anh Le, Ilse Khouw

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Case Report: Novel rare mutation c.6353C > G in the ABCA12 gene causing harlequin ichthyosis identified by whole exome sequencing by Van Khanh Tran, Quang Minh Diep, Qiu Zilong, Le Thi Phuong, Hai Anh Tran, Nguyen Van Tung, Nguyen Van Tung, Nguyen Thi Kim Lien, Nguyen Thi Xuan, Le Thi Ha, Thanh Van Ta, Thinh Huy Tran, Nguyen Huy Hoang, Nguyen Huy Hoang

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