Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
3 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
GJB2 c.-23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss.
Eur Arch Otorhinolaryngol. 2015 Sep;272(9):2255-9. doi: 10.1007/s00405-014-3171-7. Epub 2014 Jul 11.
Eur Arch Otorhinolaryngol. 2015.
PMID: 25012701
Identification of a novel mutation in congenital afibrinogenemia in Iranian patients.
Nojehdeh ST, Mojbafan M, Masoodifard M, Amini M, Zeinali S.
Nojehdeh ST, et al. Among authors: masoodifard m.
Blood Coagul Fibrinolysis. 2021 Jul 1;32(5):323-327. doi: 10.1097/MBC.0000000000001041.
Blood Coagul Fibrinolysis. 2021.
PMID: 33901106
Item in Clipboard
Frequencies of Six (Five Novel) STR Markers Linked to TUSC3 (MRT7) or NSUN2 (MRT5) Genes Used for Homozygosity Mapping of Recessive Intellectual Disability.
Ghadami S, Mohammadi HM, Malbin J, Masoodifard M, Sarhaddi AB, Tavakkoly-Bazzaz J, Zeinali S.
Ghadami S, et al. Among authors: masoodifard m.
Clin Lab. 2015;61(8):925-32. doi: 10.7754/clin.lab.2015.150101.
Clin Lab. 2015.
PMID: 26427135
Item in Clipboard
Cite
Cite