Polymorphism of MUC1 Gene in Vietnamese Gastric Cancer Patients: A Multicenter Case–Control Study by Ngoc-Lan Thi Nguyen, Ngoc-Lan Thi Nguyen, Ngoc-Dzung Thi Dang, Ngoc-Dzung Thi Dang, Quang-Huy Dang, Van-Chuc Tran, Hoang-Long Vo, Masamitsu Yamaguchi, Thanh-Van Ta, Thanh-Van Ta

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Nutritional Status, Refeeding Syndrome and Some Associated Factors of Patients at COVID-19 Hospital in Vietnam by Linh Thuy Nguyen, Thanh Van Ta, An Tuong Bui, Sy Nam Vo, Ngoc-Lan Thi Nguyen

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Merosin-deficient congenital muscular dystrophy type 1a: detection of LAMA2 variants in Vietnamese patients by Van Khanh Tran, Ngoc-Lan Nguyen, Lan Ngoc Thi Tran, Phuong Thi Le, Anh Hai Tran, Tuan L. A. Pham, Nguyen Thi Kim Lien, Nguyen Thi Xuan, Le Tat Thanh, Thanh Van Ta, Thanh Van Ta, Thinh Huy Tran, Thinh Huy Tran, Huy-Hoang Nguyen, Huy-Hoang Nguyen

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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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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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Targeted next‐generation sequencing determined a novel SGCG variant that is associated with limb‐girdle muscular dystrophy type 2C: A case report by Nam‐Chung Tran, Tuan Anh Nguyen, Thanh Dat Ta, Thinh Huy Tran, Phuoc‐Dung Nguyen, Chi Dung Vu, Van‐Hung Nguyen, The‐Hung Bui, Thanh Van Ta, Van Khanh Tran

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Family based and case–control designs reveal an association of TFAP2A in nonsyndromic cleft lip only among Vietnamese population by Duc Minh Nguyen, Satoshi Suzuki, Hideto Imura, Teruyuki Niimi, Hiroo Furukawa, Thanh‐Van Ta, Son Minh Tong, Tra Thu Nguyen, Loc Nguyen Gia Pham, Duy Le Tran, Nagato Natsume

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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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Association of the STAT4, CDKN1A, and IRF5 variants with risk of lupus nephritis and renal biopsy classification in patients in Vietnam by Trung Dung Nghiem, Gia Tuyen Do, Long Hoang Luong, Quy Linh Nguyen, Ha Viet Dang, Anh Nguyen Viet, Thuy Thu Nguyen, Van Khanh Tran, Thanh Van Ta, Thinh Huy Tran

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Feasibility of combining short tandem repeats (STRs) haplotyping with preimplantation genetic diagnosis (PGD) in screening for beta thalassemia by Vu Viet Ha Vuong, Thinh Huy Tran, Phuoc-Dung Nguyen, Nha Nguyen Thi, Phuong Le Thi, Dang Thi Minh Nguyet, Manh-Ha Nguyen, The-Hung Bui, Thanh Van Ta, Van-Khanh Tran

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Feasibility of combining short tandem repeats (STRs) haplotyping with preimplantation genetic diagnosis (PGD) in screening for beta thalassemia. by Vu Viet Ha Vuong, Thinh Huy Tran, Phuoc-Dung Nguyen, Nha Nguyen Thi, Phuong Le Thi, Dang Thi Minh Nguyet, Manh-Ha Nguyen, The-Hung Bui, Thanh Van Ta, Van-Khanh Tran

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<i>BRCA1/2</i> Mutations in Vietnamese Patients with Hereditary Breast and Ovarian Cancer Syndrome by Trong-Nhan N. Le, Van-Khanh Tran, Thu-Thuy Nguyen, Nam S. Vo, Tham H. Hoang, Hoang-Long Vo, Thanh-Hai T. Nguyen, Phuoc-Dung Nguyen, Viet-Tien Nguyen, Thanh-Van Ta, Huy-Thinh 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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In silico validation revealed the role of SCN5A mutations and their genotype–phenotype correlations in Brugada syndrome by Hung Manh Pham, Duy Phuong Nguyen, Thanh Dat Ta, Thi Phuong Le, Phong Hai Phan, Hoai An Trinh, Tuan Viet Tran, Thi Lan Anh Luong, Ha Minh Nguyen, The‐Hung Bui, Thinh Huy Tran, Thanh Van Ta, Van‐Khanh Tran

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Mutation spectrum of retinoblastoma patients in Vietnam by Dao Nguyen Ha Linh, Nguyen Van Huy, Phuoc‐Dung Nguyen, Phuong Le Thi, Hoang Anh Tuan, Trong Van Nguyen, Thu Ha Tran, Hai Anh Tran, Thanh Dat Ta, Tuan L. A. Pham, The‐Hung Bui, Thinh Huy Tran, Thanh Van Ta, Van‐Khanh Tran

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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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