Zobrazeno 1 - 2 of 2 pro vyhledávání: '"Leila Khoramifar"'
1
Akademický článek
Study of common chromosomal abnormalities and Plasminogen activator Inhibitor(PAI-1) gene Polymorphism (5G/4G) and Prothrombin (F2)gene mutation(G20210A) in women with recurrent abortions in the North West of Iran
Autor: Roya Bagheri, Seyed ali Rahmani, Leila Khoramifar, Solmaz Ilkhichoui
Publikováno v: مجله پزشکی دانشگاه علوم پزشکی تبریز, Vol 43, Iss 5, Pp 400-409 (2021)
Background. Parental chromosomal abnormalities as well as changes in genes encoding thrombophilic factors are common causes of recurrent abortions. One of the causes of thrombophilia is Factor II (F2) gene mutation (G20210A) and plasminogen activator
Externí odkaz: https://doaj.org/article/a58a8cffb1fe4e7abf4d4acce4cbe93b
Zobrazit plný text záznamu
2
Study of common chromosomal abnormalities and Plasminogen activator Inhibitor(PAI-1) gene Polymorphism (5G/4G) and Prothrombin (F2)gene mutation(G20210A) in women with recurrent abortions in the North West of Iran
Autor: Solmaz Ilkhichoui, Leila Khoramifar, Roya Bagheri, Seyed Ali Rahmani
Publikováno v: Medical Journal of Tabriz University of Medical Sciences. 43:400-409
Background. Parental chromosomal abnormalities as well as changes in genes encoding thrombophilic factors are common causes of recurrent abortions. One of the causes of thrombophilia is Factor II (F2) gene mutation (G20210A) and plasminogen activator
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1296b28b0e5b441e2e4db467c8ed4c95
https://doi.org/10.34172/mj.2021.066
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje