AHEAD OF PRINT
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
Flexural Behavior of Concrete-Filled Steel Tube CFST Members with Initial Imperfections Due to Steel Tube Notches
Haider A. A. Al-Atabi, Ahmed A. M. Al-Shaar
Association of CYP2B6 and OPRM1 Genotypes with Methadone Dose Requirements and Serum Concentrations in a Vietnamese Cohorts
Quynh Giao Nguyen, Khanh Chi Tran, Thi Phuong Dung Trinh, Huy Tan Pham, Thi Ngoc Dung Dang
Molecular and Immunohistochemical Biomarkers in Colorectal Carcinoma - A Single Center Study
B Krsteska, V Filipovski, K Kubelka-Sabit, Dz Jasar, N Velickova
Flow Cytometry Multiplex Bead Array Technology and Its Immunological Clinical Applications in Covid-19 Era
I Pavlovski, EM Riachi, S Macha, N Atanasova-Pancevska
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
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
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
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
Nephrotic Syndrome Induced by Tiopronin in a Male Patient with Cystinuria
V Karanfilovski, A Severova Stojanoska, V Ristovska, J Gjorgjievska, V Tasic, T Arsov, P Dzekova-Vidimliski, D Plaseska-Karanfilska, I Nikolov, N Gjorgjievski
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