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
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
G Protein-Coupled Receptor 35 Holds Potential as a Beacon of Hope for Treating Chondrosarcoma
A Tuncal, R Kalkan
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
First Report of a Familiar MYCBP2 Pathogenic Variant: Expanding the Knowledge of Neurodevelopmental Disorders
I Maleva Kostovska, P Noveski, E Sukarova-Angelovska, D Plaseska-Karanfilska
X-Linked Adrenoleukodystrophy in a Moroccan Patient: Genetic Diagnosis Leads to Presymptomatic Testing and Family Counseling
M Mansouri, T Smol, N Louhabe, M Rama, N Rada, N Fdil, M Bouskraoui, N Aboussair
Strengthening of Ultra-High Performance Concrete Beams with CFRP Strips
Ali Khalid Ahmed, Mustafa Hameed Al-Allaf
Current State and Challenges of Road Bridges in Italy, Portugal, and Slovakia
José C. Matos, Vanni Nicoletti, Jakub Kraľovanec, Hélder S. Sousa, Maria J. Morais, Fabrizio Gara, Martin Moravčík
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
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
