Detalhe da pesquisa
1.
Coexistence of a Homozygous Chromosome 4q35.2 Deletion and Hidden IQSEC2 Pathogenic Variant in a Child with Intellectual Disability.
Cytogenet Genome Res
; 161(3-4): 153-159, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34229322
2.
Mixed gonadal dysgenesis in a patient with de novo tas(Y;19)(p11.3;q13.4) and 45,X mosaicism.
Eur J Pediatr
; 172(9): 1215-9, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23652939
3.
Evaluation of exonic copy numbers of SMN1 and SMN2 genes in SMA.
Gene
; 823: 146322, 2022 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35219815
4.
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.
Am J Hum Genet
; 83(1): 106-11, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18565486
5.
Conventional Cytogenetics and Interphase Fluorescence In Situ Hybridization Results in Multiple Myeloma: A Turkey Laboratory Analysis of 381 Cases.
Indian J Hematol Blood Transfus
; 36(2): 284-291, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-32425379
6.
Subtelomeric rearrangements of dysmorphic children with idiopathic mental retardation reveal 8 different chromosomal anomalies.
Turk J Pediatr
; 51(5): 453-9, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-20112600
7.
Clonal evolution of monosomy 7 in acquired severe aplastic anemia: Two cases treated with allogeneic hematopoietic stem cell transplantation.
Turk J Haematol
; 25(2): 94-7, 2008 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27264447
8.
Celiac disease in patients with Williams-Beuren syndrome.
Turk J Pediatr
; 57(6): 599-604, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-27735799
9.
A Novel Coincidence: Essential Thrombocythemia with Facioscapulohumeral Muscular Dystrophy
Turk J Haematol
; 37(4): 306-307, 2020 Nov 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-32812416
10.
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
11.
Multidirectional and simultaneous evaluation of gastroschisis-related intestinal damage in chick embryos.
J Pediatr Surg
; 49(11): 1577-84, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25475797
12.
Investigation of MDM2 Oncogene Copy Number Alterations in Cases of Chronic Lymphocytic Leukemia
Turk J Haematol
; 36(2): 126-127, 2019 May 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30322832
13.
The Coexistence of Chronic Lymphocytic Leukemia and Multiple Myeloma
Turk J Haematol
; 36(2): 124-125, 2019 May 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29923494
14.
Previously Unreported Chromosomal Aberrations of t(3;3)(q29;q23), t(4;11)(q21;q23), and t(11;18)(q10;q10) in a Patient with Accelerated Phase Ph+ CML.
Case Rep Genet
; 2014: 582016, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24711936
15.
Array comparative genomic hybridization analysis of adult acute leukemia patients.
Cancer Genet Cytogenet
; 197(2): 122-9, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20193845
16.
AZF microdeletions on the Y chromosome of infertile men from Turkey.
Ann Genet
; 47(1): 61-8, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15050875
17.
Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1).
Am J Hum Genet
; 72(2): 429-37, 2003 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-12524598