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Current State and Challenges of Road Bridges in Italy, Portugal, and Slovakia
Article

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
Article

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
The Development of a Fuzzy Logic System Using MATLAB for Early Detection of Hereditary Cancer in BRCA1/2 Negative Cases
Article

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
Novel KIF11 Variants with New Clinical Features: Expanding the Clinical Phenotype
Article

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
Partial Trisomy of Chromosome 9 Inherited by Adjacent Segregation 2 of a Balanced Reciprocal Translocation in the Mother: Rare Mechanism in Chromosomal Abnormalities
Article

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
Nephrotic Syndrome Induced by Tiopronin in a Male Patient with Cystinuria
Article

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
First Report of a Familiar MYCBP2 Pathogenic Variant: Expanding the Knowledge of Neurodevelopmental Disorders
Article

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
Article

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
Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review
Article

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
Article

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
Article

Flow Cytometry Multiplex Bead Array Technology and Its Immunological Clinical Applications in Covid-19 Era

I Pavlovski, EM Riachi, S Macha, N Atanasova-Pancevska
Molecular and Immunohistochemical Biomarkers in Colorectal Carcinoma - A Single Center Study
Article

Molecular and Immunohistochemical Biomarkers in Colorectal Carcinoma - A Single Center Study

B Krsteska, V Filipovski, K Kubelka-Sabit, Dz Jasar, N Velickova