Detalhe da pesquisa
1.
A familial interstitial 4q35 deletion with no discernible clinical effects.
Am J Med Genet A
; 167A(8): 1836-41, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25846895
2.
Absence of the SLC22A12 gene mutation in Turkish population with primary gout disease.
Rheumatol Int
; 33(11): 2921-5, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23129426
3.
Pure and complete 12p trisomy due to a maternal centric fission of chromosome 12.
Am J Med Genet A
; 155A(2): 349-52, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21271652
4.
Prenatal diagnosis of ß-thalassemia and other hemoglobinopathies in southwestern Turkey.
Hemoglobin
; 35(1): 47-55, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21250881
5.
We can Diagnose it if we Consider it. Diagnostic Pitfall for Placenta: Placental Mesenchymal Dysplasia.
Turk Patoloji Derg
; 34(1): 100-103, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-28272653
6.
Maternal origin and clinical findings in a case with trisomy 22.
Turk J Pediatr
; 49(3): 322-6, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17990591
7.
An unusual case of chromosome 22q11 deletion syndrome with psychiatric disorder, hypoparathyroidism and precocious puberty.
J Pediatr Endocrinol Metab
; 19(5): 761-4, 2006 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-16789644
8.
Chromosome abnormalities identified in 457 spontaneous abortions and their histopathological findings.
Turk Patoloji Derg
; 31(2): 111-8, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25944391
9.
Rare structural chromosomal abnormalities in prenatal diagnosis; clinical and cytogenetic findings on 10125 prenatal cases.
Turk Patoloji Derg
; 31(1): 36-44, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25301051
10.
Exceptional complex chromosomal rearrangement and microdeletions at the 4q22.3q23 and 14q31.1q31.3 regions in a patient with azoospermia.
Gene
; 512(1): 157-60, 2013 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23031811
11.
A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement.
Gene
; 516(1): 176-80, 2013 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23262338
12.
A patient with Down syndrome with a de novo derivative chromosome 21.
Gene
; 507(2): 159-64, 2012 Oct 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22827956
13.
Aberrations of chromosomes 9 and 22 in acute lymphoblastic leukemia cases detected by ES-fluorescence in situ hybridization.
Genet Test Mol Biomarkers
; 16(5): 318-23, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22360868