Detalhe da pesquisa
1.
Energy Status of Lymphocytes in Children with Bronchial Asthma of Various Severity in Comparison with Frequently Ill and Healthy Children.
Bull Exp Biol Med
; 173(6): 723-729, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36322305
2.
[Effects of the Airway Obstruction on the Skin Microcirculation in Patients with Bronchial Asthma].
Vestn Ross Akad Med Nauk
; 71(3): 233-9, 2016.
Artigo
em Russo
| MEDLINE | ID: mdl-29297639
3.
Comparative cytogenetic mapping of rRNA genes among naked catfishes: implications for genomic evolution in the Bagridae family.
Genet Mol Res
; 13(4): 9533-42, 2014 Nov 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-25501163
4.
Clinical impact of somatic mosaicism in cases with small supernumerary marker chromosomes.
Cytogenet Genome Res
; 139(3): 158-63, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23295254
5.
Small supernumerary marker chromosomes (sSMC) - what about the genotype-phenotype correlation?
Tsitologiia
; 55(3): 165-6, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23795458
6.
Murine multicolor banding.
Tsitologiia
; 55(4): 259-60, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23875460
7.
Human Ring Chromosomes - New Insights for their Clinical Significance.
Balkan J Med Genet
; 16(1): 13-20, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24265580
8.
Five novel locations of Neocentromeres in human: 18q22.1, Xq27.1â¼27.2, Acro p13, Acro p12, and heterochromatin of unknown origin.
Cytogenet Genome Res
; 136(3): 163-6, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22377933
9.
Tetrasomy 9p mosaicism associated with a normal phenotype in two cases.
Cytogenet Genome Res
; 136(4): 237-41, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22487875
10.
Clinical impact of proximal autosomal imbalances.
Balkan J Med Genet
; 15(2): 15-22, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24052727
11.
Rhodobacter capsulatus PG Lipopolysaccharide Blocks the Effects of a Lipoteichoic Acid, a Toll-Like Receptor 2 Agonist.
Acta Naturae
; 14(4): 69-74, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36694898
12.
Is there a yet unreported unbalanced chromosomal abnormality without phenotypic consequences in proximal 4p?
Cytogenet Genome Res
; 132(1-2): 121-3, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-20639618
13.
First case of a neocentromere formation in an otherwise normal chromosome 7.
Cytogenet Genome Res
; 128(4): 189-91, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20029167
14.
The case of an infertile male with an uncommon reciprocal X-autosomal translocation: how does this affect male fertility?
Genet Couns
; 21(4): 397-404, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-21290969
15.
Partial deletion of the long arm of chromosome 13 (q32q33.2) associated with mental retardation, choanal atresia and fish mouth.
Genet Couns
; 21(3): 317-24, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20964123
16.
A neocentric isochromosome Yp present as additional small supernumerary marker chromosome--evidence against U-type exchange mechanism?
Cytogenet Genome Res
; 125(2): 115-6, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19729914
17.
Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
Cytogenet Genome Res
; 125(2): 109-14, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19729913
18.
10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences.
Cytogenet Genome Res
; 124(1): 102-5, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19372675
19.
Array painting using microdissected chromosomes to map chromosomal breakpoints.
Cytogenet Genome Res
; 116(3): 158-66, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17317954
20.
Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literature.
Cytogenet Genome Res
; 118(1): 31-7, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17901697