A Study on Construction Schedule Management Methods under Disruptive Conditions Based on Combinatorial Thinking
Jingyi Chen, Zhengfeng Ma, Chen Yang, Jiangyu Xiong, Haoyun Yang
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
N Senturk, GP Volkan, Babiker Ali SM, B Dogan, L Aliyeva, OS Sag, G S Temel, M Dundar, C M Ergoren
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
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
Flow Cytometry Multiplex Bead Array Technology and Its Immunological Clinical Applications in Covid-19 Era
I Pavlovski, EM Riachi, S Macha, N Atanasova-Pancevska
Impact of Solid Fuel Use on Household Air Pollution and Respiratory Health in Two Low‑Income Communities in Mpumalanga, South Africa
Bianca Wernecke, Kristy Langerman, Angela Mathee, Nada Abdelatif, Marcus A. Howard, Nkosana Jafta, Christiaan Pauw, Shumani Phaswana, Kareshma Asharam, Ishen Seocharan, Hendrik Smith, Rajen N. Naidoo, Natasha Naidoo, Caradee Y. Wright
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
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
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
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