Strengthening of Ultra-High Performance Concrete Beams with CFRP Strips
Ali Khalid Ahmed, Mustafa Hameed Al-Allaf
The Expression Profile of Wnt/β-Catenin Signalling Pathway Genes in Miscarriages
E Gulseren, C B A Garber, T Hamad Al, A C Ozay, G Mocan, G S Temel, C M Ergoren
Novel KIF11 Variants with New Clinical Features: Expanding the Clinical Phenotype
T Apuhan, A Saglam Kubra, M Yilmaz, O Bebek, S.A Demiroglu, O Demir, H.A Cebi, A Turkyilmaz
Qualitative and Quantitative Aspects of Discrepancies between Various Methods for Microsatellite Instability Detection
M Staninova-Stojovska, N Matevska-Geshkovska, E Krstevska-Bozhinovikj, R Jovanovic, K Kubelka Sabit, B Angelovska, N Mitreski, P Noveski, A Dimovski
Partial Trisomy of Chromosome 9 Inherited by Adjacent Segregation 2 of a Balanced Reciprocal Translocation in the Mother: Rare Mechanism in Chromosomal Abnormalities
K Zerrouki, F E Aouni, F Smaili, J Ahmidi, S Meziane, K Ahmidouch, M Tajir
The Development of a Fuzzy Logic System Using MATLAB for Early Detection of Hereditary Cancer in BRCA1/2 Negative Cases
N Senturk, GP Volkan, Babiker Ali SM, B Dogan, L Aliyeva, OS Sag, G S Temel, M Dundar, C M Ergoren
Investigation of the Frequency of CRP Gene Polymorphism in Rheumatoid Arthritis and Associations with CRP Level and Clinical Involvements of the Disease
S Biter, I Turk, G Varkal, S Dinkçi, E Erken
Flow Cytometry Multiplex Bead Array Technology and Its Immunological Clinical Applications in Covid-19 Era
I Pavlovski, EM Riachi, S Macha, N Atanasova-Pancevska
Combined Experimental and Simulation Study on the Post-Fire Performance of RC Columns
Cherif Guergah, Malek Hamda, Mohammed Baghdadi, Abdelaziz Benmarce
Flexural Behaviour of Lightly Reinforced Concrete Beams Utilizing Graphene Oxide Powder
Sultan A. Daud, Mustafa Hameed Al-Allaf, Raid A. Daud, Fahed Alrshoudi
A Two-Stage XGBoost Approach for Mapping Arable and Non-Arable Soils under Salinity Stress in Southern Iraq
Mohammed Azeez, Hisham M. Jawad Al Sharaa, Abdul Razzak T. Zboon
Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review
H Jelti, K Khabbache, S Bouressas, F Hacht, A Oulmaati, A Lamzouri