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PubMed 19624920 Clusters of multidrug-resistant Mycobacterium tuberculosis cases, Europe. Molecular surveillance of multidrug-resistant tuberculosis (MDR TB) was implemented in Europe as case reporting in 2005. For a 1.1 KB 2015-08-06 41 6 2021-12-05
PubMed 19565319 Adenosine A(2A) receptor gene (ADORA2A) variants may increase autistic symptoms and anxiety in autism spectrum disorder. Autism spectrum disorders (ASDs) are heterogeneous disorders presenting with in 1.15 KB 2025-10-02 31 29 2021-12-05
PubMed 19067809 Hemodynamic parameters and heart rate variability during a tilt test in relation to gene polymorphism of renin-angiotensin and serotonin system. PURPOSE: The aim of the study was to evaluate the renin 1.79 KB 2015-11-24 25 26 2021-12-05
PubMed 18945288 R58fs mutation in the HGD gene in a family with alkaptonuria in the UAE. This study was conducted to determine the prevalence of alkaptonuria in the UAE population and to identify the genotype of affe 1.56 KB 2015-08-06 25 14 2021-12-05
PubMed 18672102 GATA4 mutations in 486 Chinese patients with congenital heart disease. Recent studies have reported germline mutations in GATA4 gene in some types of congenital heart disease (CHD). However, the preva 1.32 KB 2015-11-24 26 37 2021-12-05
PubMed 18189233 RNASEL and RNASEL-inhibitor variation and prostate cancer risk in Afro-Caribbeans. BACKGROUND: Afro-Caribbeans from Tobago are at high risk of developing prostate cancer. This elevated risk of prostat 1.74 KB 2015-11-23 28 31 2021-12-05
PubMed 18166824 Genetic investigation of four meiotic genes in women with premature ovarian failure. OBJECTIVE: The goal of this study was to determine whether mutations of meiotic genes, such as disrupted meiotic cD 1.56 KB 2015-11-23 28 34 2021-12-05
PubMed 19276632 Mutation analysis of FOXF2 in patients with disorders of sex development (DSD) in combination with cleft palate. In contrast to disorders of sexual differentiation caused by lack of androgen productio 1.8 KB 2015-11-25 27 37 2021-12-05
PubMed 17395743 Identification of PVT1 as a candidate gene for end-stage renal disease in type 2 diabetes using a pooling-based genome-wide single nucleotide polymorphism association study. To identify genetic varian 1.54 KB 2025-10-02 47 18 2021-12-05
PubMed 17166870 Association between an endoglin gene polymorphism and systemic sclerosis-related pulmonary arterial hypertension. UNLABELLED: Systemic sclerosis (SSc) is a connective tissue disorder characterized by 1.66 KB 2015-11-23 27 41 2021-12-05