Detalhe da pesquisa
1.
Small supernumerary marker chromosome 15 and a ring chromosome 15 associated with a 15q26.3 deletion excluding the IGF1R gene.
Am J Med Genet A
; 176(2): 443-449, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29226546
2.
Significant interethnic differencies in functional variants of PON1 and P2RY12 genes in Roma and Hungarian population samples.
Mol Biol Rep
; 42(1): 227-32, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25297118
3.
[Catch-22? Wide variety of phenotypes associated with the chromosome 22q11 deletion syndrome in two patients]. / A 22-es csapdája? A 22q11 kromoszóma deletiós szindróma változatos klinikai megjelenése két eset kapcsán.
Orv Hetil
; 156(45): 1834-8, 2015 Nov 08.
Artigo
em Húngaro
| MEDLINE | ID: mdl-26522857
4.
Marked differences of haplotype tagging SNP distribution, linkage, and haplotype profile of IL23 receptor gene in Roma and Hungarian population samples.
Cytokine
; 65(2): 148-52, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24332578
5.
Admixture of beneficial and unfavourable variants of GLCCI1 and FCER2 in Roma samples can implicate different clinical response to corticosteroids.
Mol Biol Rep
; 41(11): 7665-9, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25091946
6.
[Attention deficit hyperactivity disorder analyzed with array comparative genome hybridization method. Case report]. / Figyelemhiányos hiperaktivitásban szenvedo beteg vizsgálata array komparatív genomhibridizációs módszerrel.
Orv Hetil
; 155(40): 1598-601, 2014 Oct 05.
Artigo
em Húngaro
| MEDLINE | ID: mdl-25261991
7.
[Identifying rare genomic disorders with array comparative genomic hybridization in Hungary]. / Ritka genomikai betegségek azonosítása array komparatív genomhibridizációs módszerrel - elsoként Magyarországon.
Orv Hetil
; 155(9): 358-61, 2014 Mar 02.
Artigo
em Húngaro
| MEDLINE | ID: mdl-24566700
8.
Common functional variants of APOA5 and GCKR accumulate gradually in association with triglyceride increase in metabolic syndrome patients.
Mol Biol Rep
; 39(2): 1949-55, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21643755
9.
Erratum to: Significant interethnic differences in functional variants of PON1 and P2RY12 genes in Roma and Hungarian population samples.
Mol Biol Rep
; 42(1): 317, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25366175
10.
Marked Differences of Haplotype Tagging SNP Distribution, Linkage, and Haplotype Profile of APOA5 Gene in Roma Population Samples.
Pathol Oncol Res
; 23(4): 853-861, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28102463
11.
Kleefstra syndrome in Hungarian patients: additional symptoms besides the classic phenotype.
Mol Cytogenet
; 9: 22, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26918030
12.
Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotype.
Mol Cytogenet
; 8: 41, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26110020
13.
Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome.
Mol Cytogenet
; 8: 16, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25774221
14.
Functional variants of lipid level modifier MLXIPL, GCKR, GALNT2, CILP2, ANGPTL3 and TRIB1 genes in healthy Roma and Hungarian populations.
Pathol Oncol Res
; 21(3): 743-9, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25573592
15.
Increased prevalence of functional minor allele variants of drug metabolizing CYP2B6 and CYP2D6 genes in Roma population samples.
Pharmacol Rep
; 67(3): 460-4, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25933954
16.
Hodgkin disease therapy induced second malignancy susceptibility 6q21 functional variants in roma and hungarian population samples.
Pathol Oncol Res
; 20(3): 529-33, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24306881
17.
Genetic polymorphisms in promoter and intronic regions of CYP1A2 gene in Roma and Hungarian population samples.
Environ Toxicol Pharmacol
; 38(3): 814-20, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25461540
18.
Deletion of 4q28.3-31.23 in the background of multiple malformations with pulmonary hypertension.
Mol Cytogenet
; 7: 36, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24959202