Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tuan Pham Le-Anh"'
Autor:
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
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 57, Iss 6, Pp 878-880 (2018)
Objective: Duchenne muscular dystrophy (DMD) is a severe disorder caused by mutation in the X-linked dystrophin gene, therefor carrier testing is required for all female family members. However, there are cases mutation analysis cannot detect any mut
Externí odkaz:
https://doaj.org/article/3f05c68b10114e57a4034fc50d7fb7ac
Autor:
Van Khanh Tran, Tuan Pham Le-Anh, Long Hoang Luong, Dat Quoc Tran, Thanh Van Ta, Thinh Huy Tran, The-Hung Bui, Linh Thuy Dinh, Phuong Thi Le, Duc Hinh Nguyen
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 57, Iss 6, Pp 878-880 (2018)
Objective: Duchenne muscular dystrophy (DMD) is a severe disorder caused by mutation in the X-linked dystrophin gene, therefor carrier testing is required for all female family members. However, there are cases mutation analysis cannot detect any mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::354b776d88cdd0ef45f9baa7598e473c
https://doi.org/10.1016/j.tjog.2018.10.019
https://doi.org/10.1016/j.tjog.2018.10.019
Autor:
Tuan-Pham, Le Anh, Tran, Thinh Huy, Tran, Dat Quoc, Minh, Nguyen Thi, Huong, Nguyen Lien, Tien, Nguyen Viet, Ta, Van Thanh, Bui, The Hung, Tran, Van Khanh
Microsatellite polymorphic markers were powerful tool to perform single cell diagnosis for preimplantation genetic diagnosis (PGD) in X-linked recessive disorders. This type of analysis requires haplotypes information of carrier mothers and affected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmc_________::7a38f0bb51b797cfb1682e3fe1f31067
https://europepmc.org/articles/PMC4563422/
https://europepmc.org/articles/PMC4563422/
Autor:
Tran, Van Khanh, Do, Ngoc Hai, Tran, Thinh Huy, Ta, Minh Hieu, Tuan-Pham, Le Anh, Chi, Dung Vu, Khanh, Nguyen Ngoc, Ta, Van Thanh, Matsuo, Masafumi
Duchenne/Becker muscular dystrophy (DMD/BMD) the most common X-linked muscular dystrophy is caused by mutation in dystrophin gene. Deletion and duplication in the dystrophin gene account for 60-70% of mutation. Multiplex ligation-dependent probe ampl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmc_________::0f7298006b9a6619580d06da5d381aeb
https://europepmc.org/articles/PMC4563477/
https://europepmc.org/articles/PMC4563477/