Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Huda I. ElFakharay"'
Autor:
Sana Al-Jarrash, J. Francis Borgio, Zaki A. Naserullah, Sayed AbdulAzeez, Ahmed M. Al-Suliman, Huda I. ElFakharay, Noor B. Almandil
Publikováno v:
Molecular Biology Reports. 47:603-606
In the Eastern province of Saudi Arabia, thalassemia is highly common. Data on the effect of alpha globin gene variation on the concentration of iron on transfusion dependent Saudis are scanty. A total of 166 transfusions dependent β-thalassemia wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cc7c19f77e0b5ee5390ff3076f8400a
https://doi.org/10.1007/s11033-019-05168-w
https://doi.org/10.1007/s11033-019-05168-w
Autor:
Fatimah Alabdrabalnabi, Amein Al Ali, Mohammed Shakil Akhtar, Jesu Francis Borgio, Noor B. Almandil, Sayed AbdulAzeez, Huda I. ElFakharay, Hatem O. Qutub, Ahmed Suliman, Mohammed A. AlKhalifah, Fuad Qaw, Zaki A. Naserullah, Sana Al Jarrash
Publikováno v:
Molecular medicine reports. 17(1)
The regions of Al‑Qatif and Al‑Ahssa in the Eastern Province of Saudi Arabia are known for their high prevalence of hemoglobinopathies, including β‑thalassemia and sickle cell anemia. Previously, the α‑gene deletion has been demonstrated as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2e9fe401d098a6f1f39fc154cfe4c32
https://pubmed.ncbi.nlm.nih.gov/29138844
https://pubmed.ncbi.nlm.nih.gov/29138844