Saltar al contenido
Blog EERR.es
Noticias
Artículos
Am J Hum Genet
Ann Hum Genet
Eur J Hum Genet
Frontiers in genetics
J Mol Diagn
Journal of Medical Genetics
Human Molecular Genetics
The Journal of Molecular Diagnostics
Exploring barriers to clinical trial readiness among the myotonic dystrophy community: a mixed-methods study
Jun 18, 2026
—
por
Latest Results
en
Articulos
,
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
←
Anterior:
The relationship between appetite hormones and body mass index in children with intoxication type metabolic diseases
Siguiente:
Clinical characteristics and a screening tool for VEXAS syndrome: a case-control study from China
→