Detalhe da pesquisa
1.
Is cervical swab an efficient method for developing a new noninvasive prenatal diagnostic test for numerical and structural chromosome anomalies?
Turk J Med Sci
; 51(3): 1043-1048, 2021 06 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-33315353
2.
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
3.
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
4.
A case with a ring chromosome 22.
Turk J Pediatr
; 50(2): 193-6, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18664089
5.
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
6.
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
7.
Molecular karyotyping of an isolated partial trisomy 11q patient with additional findings.
Gene
; 524(2): 355-60, 2013 Jul 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-23644025
8.
The importance of systematic genetic approach to familial schizophrenia cases and discussion of cryptic mosaic X chromosome aneuploidies in schizophrenia pathogenesis.
Int J Psychiatry Clin Pract
; 14(3): 204-11, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24917321