Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Adnène Mlika"'
Autor:
Najla Soyah, Abdelbasset Amara, Faïza Zbidi, Ilhem Charfeddine, Abdelkarim Ayedi, Ahlem M'sakni, Saoussen Abroug, Jihene Bouguila, Hechmi Ben Hamouda, Adnène Mlika, Khalid Hlel, Taheni Ben Lazreg, Ali Saad, N. Zouari, Anouar Chaieb, Lamia Boughamoura, Moez Gribaa
Publikováno v:
Hemoglobin. 39:251-255
The β hemoglobinopathies [β-thalassemia (β-thal) and structural hemoglobin (Hb) variants such as Hb S (HBB: c.20A T) and Hb E (HBB: c.79G A)] are among the most common inherited diseases worldwide. In Tunisia, due to the high prevalence of consang
Autor:
Meriam Hadj Amor, Sarra Dimassi, Amel Taj, Wafa Slimani, Hanene Hannachi, Adnene Mlika, Khaled Ben Helel, Ali Saad, Soumaya Mougou-Zerelli
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-11 (2020)
Abstract Background While Miller-Dieker syndrome critical region deletions are well known delineated anomalies, submicroscopic duplications in this region have recently emerged as a new distinctive syndrome. So far, only few cases have been described
Externí odkaz:
https://doaj.org/article/6e8d2af9d0624869a30bede1b6354a49