Detalhe da pesquisa
1.
The interrelation between the high expression level of MIR34a and the trisomic abortion materials.
J Obstet Gynaecol Res
; 50(5): 842-848, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38452772
2.
Direct embryonic biopsy with transcervical embryoscopy is an effective method for karyotyping and morphology assessment in miscarriages.
J Assist Reprod Genet
; 2024 May 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38758292
3.
[Investigation of the Relationship Between IL28B Polymorphisms and Plasma IL28B Levels in Patients with Chronic Hepatitis B or C]. / Kronik Hepatit B veya C Hastalarinda IL28B Polimorfizmleri ve Plazma IL28B Düzeyleri Arasindaki Iliskinin Arastirilmasi.
Mikrobiyol Bul
; 55(3): 374-388, 2021 Jul.
Artigo
em Turco
| MEDLINE | ID: mdl-34416803
4.
Retrospective analysis of the association of the expression and single nucleotide polymorphisms (SNPs) of the TLR4, PTX3 and Dectin-1 (CLEC/A) genes with development of invasive aspergillosis among haematopoietic stem cell transplant recipients with oncohaematological disorders.
Mycoses
; 63(8): 832-839, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32291814
5.
Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case.
Am J Med Genet A
; 164A(7): 1770-6, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24677787
6.
Prenatal diagnosis of campomelic dysplasia due to SOX9 deletion.
J Obstet Gynaecol
; 39(8): 1175-1176, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31234679
7.
The relationship between the clinical course of SARS-CoV-2 infections and ACE2 and TMPRSS2 expression and polymorphisms.
Adv Clin Exp Med
; 33(1): 39-51, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37326579
8.
Unique variant of Adams-Oliver syndrome with dilated cardiomyopathy and heart block.
Pediatr Int
; 55(4): 508-12, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23910800
9.
The effect of octreotide, an analog of somatostatin, on bleomycin-induced interstitial pulmonary fibrosis in rats.
Drug Chem Toxicol
; 36(2): 181-6, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22946449
10.
Identification of an Alu-mediated 12.2-kb deletion of the complete LPAR6 (P2RY5) gene in a Turkish family with hypotrichosis and woolly hair.
Exp Dermatol
; 21(6): 469-71, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22621192
11.
Expression of the syncytin-1 and syncytin-2 genes in the trophoblastic tissue of the early pregnancy losses with normal and abnormal karyotypes.
Gene
; 741: 144533, 2020 May 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-32145327
12.
The value of interleukin-12B (p40) gene promoter polymorphism in patients with schizophrenia in a region of East Turkey.
Psychiatry Clin Neurosci
; 62(3): 307-12, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18588591
13.
Clinical findings in cases with 9q deletion encompassing the 9q21.11q21.32 region.
Turk J Pediatr
; 60(1): 94-98, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30102487
14.
Cystic hygroma: a single-centre experience.
Singapore Med J
; 2023 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37171419
15.
Microdeletion and mutation analysis of the SHOX gene in patients with idiopathic short stature with FISH and sequencing
Turk J Med Sci
; 48(2): 386-390, 2018 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-29714459
16.
The relation between isolated micropenis in childhood with CAG and GGN repeat polymorphisms in the androgen receptor gene
Turk J Med Sci
; 48(2): 430-434, 2018 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-29714466
17.
Confirmation of the prenatal mosaic trisomy 2 via fetal USG and cytogenetic analyses.
J Matern Fetal Neonatal Med
; 30(13): 1579-1583, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27431726
18.
Tumor suppressor gene alterations in patients with malignant mesothelioma due to environmental asbestos exposure in Turkey.
J Carcinog
; 5: 23, 2006 Aug 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-16925806
19.
A Turkish family with Nance-Horan Syndrome due to a novel mutation.
Gene
; 525(1): 141-5, 2013 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23566852
20.
Cochlear involvement in Familial Mediterranean Fever: a new feature of an old disease.
Int J Pediatr Otorhinolaryngol
; 76(2): 244-7, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22177320