Showing results (31-40 of 399) with videos related to

Sort By:
Pageof 40
Balkan Journal of Medical Genetics : BJMG|September 21, 2013
Pulmonary Thromboembolism Following Radio-Frequency Ablation of the Atrioventricular Node in a Patient Heterozygous for the Factor V Leiden and the Mthfr C677T MutationsDp Pešut, Sv Raljević, Mdj Kontić, et al.
Balkan Journal of Medical Genetics : BJMG|September 21, 2013
Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangementsT Liehr, N Kosayakova, J Schröder, et al.
Balkan Journal of Medical Genetics : BJMG|September 21, 2013
The many faces of oral-facial-digital syndromeE Sukarova-Angelovska, N Angelkova, S Palcevska-Kocevska, et al.
Balkan Journal of Medical Genetics : BJMG|September 21, 2013
Muscle hemangiomatosis presenting as a severe feature in a patient with the pten mutation: expanding the phenotype of vascular malformations in bannayan-riley-ruvalcaba syndromeY Soysal, T Acun, Cm Lourenço, et al.
Balkan Journal of Medical Genetics : BJMG|September 21, 2013
16p subtelomeric duplication with vascular anomalies: an Albanian case report and literature reviewA Babameto-Laku, V Mokini, N Kuneshka, et al.
Balkan Journal of Medical Genetics : BJMG|September 21, 2013
A Preliminary microRNA Analysis of Non Syndromic Thoracic Aortic AneurysmsC Patuzzo, A Pasquali, G Malerba, et al.
Balkan Journal of Medical Genetics : BJMG|March 2, 2016
Early onset marfan syndrome: Atypical clinical presentation of two casesA Ozyurt, A Baykan, M Argun, et al.
Balkan Journal of Medical Genetics : BJMG|March 2, 2016
Congenital hydrocephalus and hemivertebrae associated with de novo partial monosomy 6q (6q25.3→qter)Y Li, K-W Choy, H-N Xie, et al.
Balkan Journal of Medical Genetics : BJMG|January 17, 2020
TWIST1 Gene Expression as a Biomarker for Predicting Primary Doxorubicin Resistance in Breast CancerS Demir, M H Müslümanoğlu, M Müslümanoğlu, et al.
Balkan Journal of Medical Genetics : BJMG|January 17, 2020
Evaluation of the JAK2V617F Mutational Burden in Patients with Philadelphia Chromosome Negative Myeloproliferative Neoplasms: A Single-center ExperienceM Popova-Labachevska, I Panovska-Stavridis, A Eftimov, et al.
Pageof 40