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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
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
AHEAD OF PRINT
Issue

AHEAD OF PRINT

Qualitative and Quantitative Aspects of Discrepancies between Various Methods for Microsatellite Instability Detection
Article

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
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
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
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
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
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
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
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
Flexural Behavior of Concrete-Filled Steel Tube CFST Members with Initial Imperfections Due to Steel Tube Notches
Article

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