Search Results - Ha Ly Thi Thanh

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    Spectrum of MECP2 mutations in Vietnamese patients with RETT syndrome by Huong Le Thi Thanh, Trinh Do Thi Diem, Chinh Vu Duy, Ha Ly Thi Thanh, Hoa Bui Thi Phuong, Liem Nguyen Thanh

    Published 2018
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  2. 2
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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

    Published 2018
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