1. Gene expression in blood from an individual with β‐thalassemia: An RNA sequence analysis. Issue 7 (27th May 2019) Authors: Taghavifar, Forough; Hamid, Mohammad; Shariati, Gholamreza Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 7(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Influence of glutathione S‐transferases (GSTM1, GSTT1, and GSTP1) genetic polymorphisms and smoking on susceptibility risk of chronic myeloid leukemia and treatment response. Issue 7 (20th May 2019) Authors: Rostami, Golale; Assad, Dlnya; Ghadyani, Fatemeh; Hamid, Mohammad; Karami, Amirhossien; Jalaeikhoo, Hasan; Kalahroodi, Ramezan Ali Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 7(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Genome‐wide single nucleotide polymorphism‐based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa. Issue 10 (19th February 2018) Authors: Vahidnezhad, Hassan; Youssefian, Leila; Saeidian, Amir Hossein; Zeinali, Sirous; Touati, Andrew; Abiri, Maryam; Sotoudeh, Soheila; Norouz‐zadeh, Sara; Amirinezhad, Niloufar; Mozafari, Nikoo; Daneshpazhooh, Maryam; Mahmoudi, Hamidreza; Hamid, Mohammad; Bradfield, Jonathan P.; Kim, Cecilia E.; Hako... Other Names: Bauer Johann W. guestEditor.; Bodemer Christine guestEditor.; Schmuth Matthias guestEditor. Journal: Experimental dermatology Issue: Volume 28:Issue 10(2019) Page Start: 1118 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Alpha‐globin gene triplication and its effect in beta‐thalassemia carrier, sickle cell trait, and healthy individual. Issue 3 (19th July 2021) Authors: Hamid, Mohammad; keikhaei, Bijan; Galehdari, Hamid; Saberi, Alihossein; Sedaghat, Alireza; Shariati, Gholamreza; Mohammadi‐Anaei, Marziye Journal: EJHaem Issue: Volume 2:Issue 3(2021) Page Start: 366 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Two Novel and Five Rare Mutations in the Non Coding Regions of the β-Globin Gene in the Iranian Population. (3rd July 2020) Authors: Hamid, Mohammad; Zargan Nezhad, Ebtesam; Keikhaei, Bijan; Galehdari, Hamid; Saberi, Alihossein; Sedaghat, Alireza; Mohammadi-Anaei, Marziye; Shariati, Gholamreza Journal: Hemoglobin Issue: Volume 44:Number 4(2020) Page Start: 225 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH. Issue 8 (13th June 2018) Authors: Shariati, Gholamreza; Saberi, Alihossein; Hamid, Mohammad; Galehdari, Hamid; Sedaghat, Alireza; Abdorasuli, Nehzat Journal: Clinical case reports Issue: Volume 6:Issue 8(2018) Page Start: 1464 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Mutation Screening of the Krüppel-like Factor 1 Gene in Individuals With Increased Fetal Hemoglobin Referred for Hemoglobinopathy Investigation in South of Iran. Issue 3 (April 2018) Authors: Hamid, Mohammad; Ershadi Oskouei, Sanaz; Shariati, Gholamreza; Babaei, Esmaeil; Galehdari, Hamid; Saberi, Alihossein; Sedaghat, Alireza Journal: Journal of pediatric hematology/oncology Issue: Volume 40:Issue 3(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Hb AHVAZ [α83(F4)Leu→Arg, CTG>CGG (α2); HBA2: c.251T>G], A New Hemoglobin Variant of the α2-Globin Gene. (October 2013) Authors: Hamid, Mohammad; Shariati, Gholamreza; Saberi, Alihossein; Galehdari, Hamid; Kaikhaei, Bijan; Mohammadi-Anaei, Marziye Journal: Hemoglobin Issue: Volume 37:Number 5(2013) Page Start: 477 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Molecular prenatal diagnosis of megalencephalic leukoencephalopathy with subcortical cysts in a child from southwest of Iran. Issue 2 (26th November 2014) Authors: Shariati, Gholamreza; Hamid, Mohammad; Saberi, Alihossein; Andashti, Behnaz; Galehdari, Hamid Journal: Clinical case reports Issue: Volume 3:Issue 2(2015:Apr.) Page Start: 114 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Effect of steroids on inflammatory markers and clinical parameters in congenital open heart surgery: a randomised controlled trial. (28th April 2015) Authors: Amanullah, Muhammad M.; Hamid, Mohammad; Hanif, Hashim M.; Muzaffar, Marium; Siddiqui, Maria T.; Adhi, Fatima; Ahmad, Khabir; Khan, Shahjahan; Hasan, Zahra Journal: Cardiology in the young Issue: Volume 26:Number 3(2016) Page Start: 506 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗