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World Journal of Gastroenterology|July 31, 2007
Frequent loss of heterozygosity at 8p22 chromosomal region in diffuse type of gastric cancerHedayat Allah Hosseini, Ali Ahani, Hamid Galehdari, et al.
Congenital Anomalies|July 17, 2021
Whole exome sequencing identified a novel frameshift variant in the BHLHA9 in an Iranian family with mesoaxial synostotic syndactylySahar Sadat Sedighzadeh, Alireza Sedaghat, Mina Zamani, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|April 11, 2014
Characterization of wild-type and mutated RET proto- oncogene associated with familial medullary thyroid cancerMohammad Hosein Masbi, Javad Mohammadiasl, Hamid Galehdari, et al.
Basic and Clinical Neuroscience|February 22, 2021
Identification of the rs797045105 in the SERAC1 Gene by Whole-exome Sequencing in a Patient Suspicious of MEGDEL SyndromeMina Zamani, Tahereh Seifi, Jawaher Zeighami, et al.
Biomed Research International|November 29, 2013
UGT1A1 gene mutation due to Crigler-Najjar syndrome in Iranian patients: identification of a novel mutationJavad Mohammadi Asl, Mohammad Amin Tabatabaiefar, Hamid Galehdari, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|September 27, 2012
Toxicological and mutagenic analysis of Artemisia dracunculus (tarragon) extractHeibatullah Kalantari, Hamid Galehdari, Zahra Zaree, et al.
Frontiers in Oncology|June 24, 2021
WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian FamilyMahnaz Norouzi, Mohammad Shafiei, Zeinab Abdollahi, et al.
Hemoglobin|July 17, 2020
Two Novel and Five Rare Mutations in the Non Coding Regions of the β-Globin Gene in the Iranian PopulationMohammad Hamid, Ebtesam Zargan Nezhad, Bijan Keikhaei, et al.
Scientific Reports|July 22, 2023
High incidence of AZF duplications in clan-structured Iranian populations detected through Y chromosome sequencing read depth analysisMogge Hajiesmaeil, Francesco Ravasini, Flavia Risi, et al.
Molecular Syndromology|February 20, 2018
Novel Homozygous Missense Mutation in RYR1 Leads to Severe Congenital Ptosis, Ophthalmoplegia, and Scoliosis in the Absence of MyopathyNafi Dilaver, Neda Mazaheri, Reza Maroofian, et al.
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