Case Report
Published on 06 Nov 2025
Case Report: Novel compound heterozygous mutations in PNPLA6 gene associated with Oliver-McFarlane syndrome
in Genetics of Common and Rare Diseases
- 838 views
Case Report
Published on 06 Nov 2025
in Genetics of Common and Rare Diseases
Original Research
Published on 06 Nov 2025
in Pediatric Oncology
Original Research
Published on 06 Nov 2025
in Movement Science
Original Research
Published on 06 Nov 2025
in Inflammation
Review
Published on 06 Nov 2025
in Alzheimer's Disease and Related Dementias
Original Research
Published on 06 Nov 2025
in Public Health Education and Promotion
Original Research
Published on 06 Nov 2025
in Cornea and Refractive Surgery
Original Research
Published on 06 Nov 2025
in Pediatric Neurology
Original Research
Published on 06 Nov 2025
in Environmental Water Quality
Original Research
Published on 06 Nov 2025
in Public Health Policy
Original Research
Published on 06 Nov 2025
in Nephrology
Original Research
Published on 06 Nov 2025
in Oral Epidemiology
Review
Published on 06 Nov 2025
in Teacher Education
Original Research
Published on 06 Nov 2025
in Health Economics
Brief Research Report
Published on 06 Nov 2025
in Developmental Psychopathology and Mental Health
Systematic Review
Published on 06 Nov 2025
in Orthopedic Surgery