Molecular Investigation of Beta Globin Gene Cluster Deletions in Anemic Patients Referred to the Genetic Laboratory of Amirkola Children Hospital (Iran)

Molecular Investigation of Beta Globin Gene Cluster Deletions in Anemic Patients Referred to the Genetic Laboratory of Amirkola Children Hospital (Iran)

BACKGROUND AND OBJECTIVE: Hereditary persistence of fetal hemoglobin (HPFH) and δβ-thalassemia are heterogeneous disorders characterized by elevated levels of fetal hemoglobin (Hb F). Deletional mutations are responsible for the disease and are not recognized by routine hematological tests. The aim...

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Bibliographic Details
Main Authors: MR Ahmadi Fard, H Akhavan Niaki, H Mahmoodi Nesheli, A Banihashemi, M Azizi, N Mousavi, R Pourbagher, R Yousefi Kamangari
Format: Article
Language:English
Published: Babol University of Medical Sciences 2012-05-01
Series:Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul
Subjects:
delta beta thalassemia
pcr
hemoglobin lepore
Online Access:http://jbums.org/article-1-4084-en.html

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http://jbums.org/article-1-4084-en.html

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