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

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BRCA1/2 Mutations in Vietnamese Patients with Hereditary Breast and Ovarian Cancer Syndrome von Le, Trong-Nhan N, Tran, Van-Khanh, Nguyen, Thu-Thuy, Vo, Nam S, Hoang, Tham H, Vo, Hoang-Long, Nguyen, Thanh-Hai T, Nguyen, Phuoc-Dung, Nguyen, Viet-Tien, Ta, Thanh-Van, Tran, Huy-Thinh

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Preventing AID, a physiological mutator, from deleterious activation: regulation of the genomic instability that is associated with antibody diversity von Nagaoka, Hitoshi, Tran, Thinh Huy, Kobayashi, Maki, Aida, Masatoshi, Honjo, Tasuku

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Feasibility of combining short tandem repeats (STRs) haplotyping with preimplantation genetic diagnosis (PGD) in screening for beta thalassemia von 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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The Plasma Levels of Protein Adiponectin ( AdipoQ ) and Meteorin-Like (Metrnl) in Newly Diagnosed Type 2 Diabetes Mellitus von Phuong, Lan Dam Thi, Tran Huy, Thinh, Huynh Quang, Thuan

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Novel mutations in the SGCA gene in unrelated Vietnamese patients with limb-girdle muscular dystrophies disease von Chung Tran, Nam, Lien, Nguyen Thi Kim, Ta, Thanh Dat, Nguyen, Van Hung, Tran, Huy Thinh, Van Tung, Nguyen, Xuan, Nguyen Thi, Huy Hoang, Nguyen, Tran, Van Khanh

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

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B cell-specific and stimulation-responsive enhancers derepress Aicda by overcoming the effects of silencers von Honjo, Tasuku, Tran, Thinh Huy, Nakata, Mikiyo, Suzuki, Keiichiro, Begum, Nasim A, Shinkura, Reiko, Fagarasan, Sidonia, Nagaoka, Hitoshi

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Treatment outcomes of EGFR-TKI with or without locoregional brain therapy in advanced EGFR-mutant non-small cell lung cancer patients with brain metastases von Linh, Do Mai, Thinh, Tran Huy, Hieu, Nguyen-Van, Duc, Nguyen Minh

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

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A case of response to combination treatment with autologous immunotherapy and bevacizumab in advanced non-small cell lung cancer von Nguyen, Thuy Mau Thi, Van Tran, Khanh, Ta, Van Thanh, Tran, Linh Mai, Tran, Chi Khanh, Trinh, Huy Le, Ta, Dat Thanh, Nguyen, Binh Thanh, Tran, Thinh Huy

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

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A case of self‐improving collodion ichthyosis in Vietnam von Diep, Quang Minh, Luong, Long Hoang, Tran, Thinh Huy, Dinh, Oanh Thi Lan, Nguyen, Hung Quoc, Bui, The‐Hung, Ta, Thanh Van, Tran, Van Khanh

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Molecular Characterization and Genotype-Phenotype Correlation of G6PD Mutations in Five Ethnicities of Northern Vietnam von Ngo, Thi Thao, Tran, Thinh Huy, Ta, Thanh Dat, Le, Thi Phuong, Nguyen, Phuoc Dung, Tran, Mai Anh, Bui, The-Hung, Ta, Thanh Van, Tran, Van Khanh

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

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

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In silico validation revealed the role of SCN5A mutations and their genotype–phenotype correlations in Brugada syndrome von Pham, Hung Manh, Nguyen, Duy Phuong, Ta, Thanh Dat, Le, Thi Phuong, Phan, Phong Hai, Trinh, Hoai An, Tran, Tuan Viet, Luong, Thi Lan Anh, Nguyen, Ha Minh, Bui, The‐Hung, Tran, Thinh Huy, Ta, Thanh Van, Tran, Van‐Khanh

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Acromesomelic dysplasia Maroteaux‐type in patients from Vietnam von Tran, Thinh Huy, Cao, My Ha, Luong, Long Hoang, Le, Phuong Thi, Vu, Dung Chi, Ta, Thanh Dat, Bui, The‐Hung, Nguyen, Duc Hinh, Van Ta, Thanh, Tran, Van Khanh

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

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

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