Negin Faramarzi Garous

Point mutations which should not be overlooked in Hb H disease

S. Farashi, H. Najmabadi, A. Azarkeivan, 2016, Expert review of hematology.

Hb Dartmouth (HBA2: c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient

S. Farashi, H. Najmabadi, A. Azarkeivan, 2015, Hemoglobin.

A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease

S. Farashi, H. Najmabadi, F. Zeinali, 2015, Hemoglobin.

Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases

H. Najmabadi, R. Kariminejad, M. Bazrgar, 2019, Molecular genetics & genomic medicine.

Copy number variations of six and seven α-globin genes in a family with intermedia and major thalassemia phenotypes

S. Farashi, H. Najmabadi, A. Azarkeivan, 2015, Expert review of hematology.

Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia

S. Farashi, H. Najmabadi, S. Zeinali, 2015, Hemoglobin.

Point mutations which should not be overlooked in Hb H disease

S. Farashi, H. Najmabadi, A. Azarkeivan, 2016, Expert review of hematology.