Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ha Ly Thi Thanh"'
Autor:
Huong Le Thi Thanh, Trinh Do Thi Diem, Chinh Vu Duy, Ha Ly Thi Thanh, Hoa Bui Thi Phuong, Liem Nguyen Thanh
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-6 (2018)
Abstract Background Rett syndrome (RTT) is a severe neurodevelopmental disorder in children characterized by a normal neurodevelopmental process in the first 6–18 months followed by a period of motor and vocal deterioration with stereotypic hand mo
Externí odkaz:
https://doaj.org/article/a324a4b140234796a39ba8d3262d991f
Autor:
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
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 57, Iss 3, Pp 435-441 (2018)
Objective: The thalassemias is a group of hereditary disorders with impaired production of functional hemoglobin. In this report we described a rare case of compound heterozygous mutation of South-East Asia type hereditary persistence of fetal hemogl
Externí odkaz:
https://doaj.org/article/eb1162ceafa8486f878114c421f0184d
Autor:
Ha Ly Thi Thanh, Hoa Bui Thi Phuong, Chinh Vu Duy, Liem Nguyen Thanh, Trinh Do Thi Diem, Huong Le Thi Thanh
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-6 (2018)
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-6 (2018)
Background Rett syndrome (RTT) is a severe neurodevelopmental disorder in children characterized by a normal neurodevelopmental process in the first 6–18 months followed by a period of motor and vocal deterioration with stereotypic hand movements.