Showing results (101-110 of 179) with videos related to

Sort By:
Pageof 18
Data in Brief|January 1, 2020
Expression analysis data of BCL11A and γ-globin genes in KU812 and KG-1 cell lines after CRISPR/Cas9-mediated BCL11A enhancer deletionMohammad Ali Khosravi, Maryam Abbasalipour, Jean-Paul Concordet, et al.
Blood Cells, Molecules & Diseases|April 6, 2010
Development of a quantitative real-time PCR assay for detection of unknown alpha-globin gene deletionsMohammad-Sadegh Fallah, Reza Mahdian, Seyyed-Ahmad Aleyasin, et al.
Ophthalmology|September 12, 2009
Variable expressivity and high penetrance of CYP1B1 mutations associated with primary congenital glaucomaFatemeh Suri, Shahin Yazdani, Mehrnaz Narooie-Nejhad, et al.
Archives of Iranian Medicine|January 4, 2011
Co-inheritance of hemoglobin D and β-thalassemia traits in three Iranian families: clinical relevanceMaryam Taghavi Basmanj, Morteza Karimipoor, Azam Amirian, et al.
European Journal of Human Genetics : EJHG|September 27, 2003
DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1Sedigheh Delmaghani, Asadollah Aghaie, Sylvie Compain-Nouaille, et al.
Blood Cells, Molecules & Diseases|October 12, 2023
First report of a patient with homozygous hemoglobin Ernz: Evidence to support a non-pathogenic variantZohreh Shojaei, Maryam Abiri, Fatemeh Zafarghandi Motlagh, et al.
Hereditas|May 29, 2023
Identifying and predicting the pathogenic effects of a novel variant inducing severe early onset MMA: a bioinformatics approachFereshteh Maryami, Elham Rismani, Elham Davoudi-Dehaghani, et al.
Scientific Reports|March 31, 2022
Efficacy and antitumor activity of a mutant type of interleukin 2Rada Dehghan, Arezoo Beig Parikhani, Sirous Zeinali, et al.
JIMD Reports|June 2, 2016
Four Years of Diagnostic Challenges with Tetrahydrobiopterin Deficiencies in Iranian PatientsShohreh Khatami, Soghra Rouhi Dehnabeh, Sirous Zeinali, et al.
Pageof 18