Detalhe da pesquisa
1.
Clinical and Histopathological Features of Gelsolin Amyloidosis Associated with a Novel GSN Variant p.Glu580Lys.
Int J Mol Sci
; 22(3)2021 Jan 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-33499149
2.
A case of avoidable heterotopic pregnancy after single embryo transfer.
Reprod Biomed Online
; 30(6): 622-4, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25892502
3.
Multisite Verification of a Targeted CFTR Polymerase Chain Reaction/Capillary Electrophoresis Assay That Evaluates Pathogenic Variants Across Diverse Ethnic and Ancestral Groups.
Arch Pathol Lab Med
; 2024 Jan 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38190268
4.
A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study.
PLoS One
; 18(12): e0294969, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38051749
5.
A multicenter study of genetic testing for Parkinson's disease in the clinical setting.
NPJ Parkinsons Dis
; 8(1): 149, 2022 Nov 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36333361
6.
The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy.
Mol Genet Genomic Med
; 7(6): e658, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31004418
7.
Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss.
PLoS One
; 13(1): e0188578, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29293505
8.
Functional impairment of precerebral arteries in Huntington disease.
J Neurol Sci
; 372: 363-368, 2017 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27817854
9.
Frequency of HFE gene mutations C282Y and H63D in Bosnia and Herzegovina.
Coll Antropol
; 30(3): 555-7, 2006 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17058523
10.
Deletion/Deletion genotype of angiotensin-I converting enzyme gene is not associated with coronary artery disease in caucasians with type 2 diabetes.
Coll Antropol
; 29(1): 149-52, 2005 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-16117314
11.
Direct-to-consumer genetic testing in Slovenia: availability, ethical dilemmas and legislation.
Biochem Med (Zagreb)
; 25(1): 84-9, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25672471
12.
The -429 T/C and -374 T/A gene polymorphisms of the receptor of advanced glycation end products gene (RAGE) are not risk factors for coronary artery disease in Slovene population with type 2 diabetes.
Coll Antropol
; 28(2): 611-6, 2004 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-15666591
13.
The ScaI gene polymorphism of the atrial natriuretic factor and essential arterial hypertension in childhood.
Coll Antropol
; 28(2): 617-21, 2004 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-15666592
14.
Insertion/deletion polymorphism of angiotensin-converting enzyme gene--risk factor for coronary artery disease in the Tuzla region population (Bosnia and Herzegovina).
Coll Antropol
; 27(2): 537-40, 2003 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-14746140
15.
Analysis of the CAG repeat number in exon 1 of the androgen receptor gene in Slovene men with idiopathic azoospermia and oligoasthenoteratozoospermia.
Asian J Androl
; 9(2): 280-2, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17334597
16.
Androgen receptor gene (CAG)n polymorphism in patients with polycystic ovary syndrome.
Fertil Steril
; 90(3): 860-3, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18555222
17.
The (TAAAA)n microsatellite polymorphism in the SHBG gene influences serum SHBG levels in women with polycystic ovary syndrome.
Hum Reprod
; 22(4): 1031-6, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17189294
18.
Patients with primary cataract as a genetic pool of DMPK protomutation.
J Hum Genet
; 52(2): 123-128, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17146587
19.
No association between the microsatellite polymorphism (TTTTA)n in the promoter of the CYP11A gene and ovarian hyperstimulation syndrome.
J Assist Reprod Genet
; 23(1): 29-32, 2006 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-16391898
20.
CTG amplification in the DM1PK gene is not associated with idiopathic male subfertility.
Hum Reprod
; 19(9): 2084-7, 2004 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-15284213