Detalles de la búsqueda
1.
Impact of a Missense Variation (p.S150R:AGC>AGG) in the XRCC2 Gene on Susceptibility to Colorectal Cancer.
Clin Lab
; 64(3): 233-237, 2018 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29739106
2.
Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort.
Genet Med
; 18(4): 364-71, 2016 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-26226137
3.
Design of a biological method for rapid detection of presence of PCR inhibitors in aged bone DNA.
Clin Lab
; 58(7-8): 681-6, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-22997968
4.
Unexpected heterogeneity due to recessive and de novo dominant mutations of GJB2 in an Iranian family with nonsyndromic hearing loss: implication for genetic counseling.
Biochem Biophys Res Commun
; 402(2): 305-7, 2010 Nov 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-20937258
5.
Investigation of GJB6 large deletions in Iranian patients using quantitative real-time PCR.
Clin Lab
; 56(9-10): 467-71, 2010.
Artículo
en Inglés
| MEDLINE | ID: mdl-21086793
6.
Examination of methylation changes of VIM, CXCR4, DOK7, and SPDEF genes in peripheral blood DNA in breast cancer patients.
Indian J Cancer
; 55(4): 366-371, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-30829272
7.
Examination of methylation changes of VIM, CXCR4, DOK7, and SPDEF genes in peripheral blood DNA in breast cancer patients
Indian J Cancer
; 2018 Oct; 55(4): 366-371
Artículo
| IMSEAR | ID: sea-190391
8.
A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect.
Int J Pediatr Otorhinolaryngol
; 77(5): 821-6, 2013 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-23523375
9.
Screening of OTOF mutations in Iran: a novel mutation and review.
Int J Pediatr Otorhinolaryngol
; 76(11): 1610-5, 2012 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-22906306
10.
Impact of consanguineous marriages in GJB2-related hearing loss in the Iranian population: a report of a novel variant.
Genet Test Mol Biomarkers
; 15(7-8): 489-93, 2011.
Artículo
en Inglés
| MEDLINE | ID: mdl-21388256
11.
High level of intrafamilial phenotypic variability of non-syndromic hearing loss in a Lur family due to delE120 mutation in GJB2 gene.
Int J Pediatr Otorhinolaryngol
; 74(9): 1089-91, 2010 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-20609484
Resultados
1 -
11
de 11
1
Próxima >
>>