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1.
Expression of ERBB gene family in females with breast cancer and its correlation with clinicopathological characteristics of the disease.
Mol Biol Rep
; 49(9): 8547-8553, 2022 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-35763181
2.
BOD1 Is Required for Cognitive Function in Humans and Drosophila.
PLoS Genet
; 12(5): e1006022, 2016 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-27166630
3.
Deep sequencing reveals 50 novel genes for recessive cognitive disorders.
Nature
; 478(7367): 57-63, 2011 Sep 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-21937992
4.
Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humans.
Proc Natl Acad Sci U S A
; 108(30): 12390-5, 2011 Jul 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-21734151
5.
Phenotypical characterization of 13q deletion syndrome: Report of two cases.
Indian J Hum Genet
; 20(2): 203-5, 2014 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-25400354
6.
Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization.
Indian J Hum Genet
; 19(4): 443-8, 2013 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-24497710
7.
A novel mutation in MCPH1 gene in an Iranian family with primary microcephaly.
J Pak Med Assoc
; 62(11): 1244-7, 2012 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-23866422
8.
Exploring the Genetic Causality of Discordant Phenotypes in Familial Apparently Balanced Translocation Cases Using Whole Exome Sequencing.
Genes (Basel)
; 14(1)2022 12 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-36672823
9.
Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots.
Hum Genet
; 129(2): 141-8, 2011 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-21063731
10.
A defect in the TUSC3 gene is associated with autosomal recessive mental retardation.
Am J Hum Genet
; 82(5): 1158-64, 2008 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-18452889
11.
Prenatal diagnosis in a mentally retarded woman with mosaic ring chromosome 18.
Indian J Hum Genet
; 17(2): 111-3, 2011 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-22090726
12.
The Relationship between KIT Copy Number Variation, Protein Expression, and Angiogenesis in Sporadic Breast Cancer.
Rep Biochem Mol Biol
; 9(1): 40-49, 2020 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-32821750
13.
Investigation of Aneusomy of Chromosome 21 in the Micronuclei of 13 Patients with Early Onset Alzheimer's Disease Using Fluorescence in Situ Hybridization: A Pilot Study.
Rep Biochem Mol Biol
; 8(4): 446-453, 2020 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-32582804
14.
Whole-Exome Sequencing Identifies Three Candidate Homozygous Variants in a Consanguineous Iranian Family with Autism Spectrum Disorder and Skeletal Problems.
Mol Syndromol
; 11(2): 62-72, 2020 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-32655337
15.
Bi-allelic Mutations in ALDH5A1 is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability.
Gene
; : 144918, 2020 Jul 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32621952
16.
Combination of Genetics and Nanotechnology for Down Syndrome Modification: A Potential Hypothesis and Review of the Literature.
Iran J Public Health
; 48(3): 371-378, 2019 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-31223563
17.
A Pathogenic Homozygous Mutation in The Pleckstrin Homology Domain of RASA1 Is Responsible for Familial Tricuspid Atresia in An Iranian Consanguineous Family.
Cell J
; 21(1): 70-77, 2019 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-30507091
18.
Application of Multiplex Ligation-Dependent Probe Amplification in Determining the Copy Number Alterations of HER Gene Family Members in Invasive Ductal Breast Carcinoma.
Rep Biochem Mol Biol
; 8(1): 91-101, 2019 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-31334294
19.
A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East.
Front Pediatr
; 7: 89, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-30949462
20.
Investigation of CEBPA and CEBPA-AS Genes Expression in Acute Myeloid Leukemia.
Rep Biochem Mol Biol
; 7(2): 136-141, 2019 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-30805392