Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Achraf LAGHMICH"'
Autor:
Mohcine Bennani-Mechita, Achraf Laghmich, Naima Ghailani-Nourouti, Amina Barakat, Fatima-Zahra Alaoui-Ismaili
Publikováno v:
Hemoglobin. 44:190-194
Sickle cell disease is one of the most common severe monogenic disorders in the world. The -158 XmnI polymorphism (C>T) of the Gγ-globin gene promoter is known to be associated with increased expression of the Gγ-globin gene, thus, higher productio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79897edc0cd044d7c981c50d01c803ec
https://doi.org/10.1080/03630269.2020.1772284
https://doi.org/10.1080/03630269.2020.1772284
Autor:
Fatima Zahra Alaoui, Achraf LAGHMICH, Naima GHAILANI NOUROUTI, Amina BARAKAT, Mohcine BENNANI MECHITA
Background: Hemoglobinopathies are the most frequent widely spread genetic disorders. In Morocco, epidemiological and clinical data are scarce. The present study aims to determine the spectrum and geographic distribution of hemoglobinopathies in Lara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::766b0b242d1f601a12c1c31d568b3da8
https://doi.org/10.21203/rs.3.rs-62915/v1
https://doi.org/10.21203/rs.3.rs-62915/v1
Autor:
Achraf Laghmich, Mohamed Khattab, Amina Barakat, Naima Ghailani Nourouti, Fatima Zahra Alaoui Ismaili, Mohcine Bennani Mechita
Publikováno v:
BioMed Research International, Vol 2019 (2019)
BioMed Research International
BioMed Research International
Unlike the other hemoglobinopathies, few researches have been published concerningα-thalassemia in Morocco. The epidemiological features and the mutation spectrum of this disease are still unknown. This regional newborn screening is the first to stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb1905fb3348078c8f325df581921433
https://doaj.org/article/cebb227a584546a2a2afd4ae640c29b8
https://doaj.org/article/cebb227a584546a2a2afd4ae640c29b8
Autor:
Amina Barakat, Mohcine Bennani Mechita, Achraf Laghmich, Fatima Zahra Alaoui Ismaili, Naima Ghailani Nourouti, Zeineb Zian
Publikováno v:
BioMed Research International, Vol 2019 (2019)
BioMed Research International
BioMed Research International
Consanguinity is a social behavior characterized by the arrangement of marriages between relatives. It coincides generally with the geographic distribution of recessive genetic diseases as it increases the likelihood of homozygosis and, consequently,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db3d1007efe74d0968d2381fca32d837
https://doaj.org/article/119e2b9519ae4f56984ea5f60d47c987
https://doaj.org/article/119e2b9519ae4f56984ea5f60d47c987