Cargando…
Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population
Autores principales: | Muroke, Valtteri, Jalanko, Mikko, Ruotsalainen, Sanni, Perola, Markus, Helle, Emmi, Sinisalo, Juha |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581411/ https://www.ncbi.nlm.nih.gov/pubmed/37577800 http://dx.doi.org/10.1161/CIRCGEN.123.004070 |
Ejemplares similares
-
Cause‐Specific Mortality of Patients With Atrial Septal Defect and Up to 50 Years of Follow‐Up
por: Muroke, Valtteri, et al.
Publicado: (2023) -
Non-invasive dye dilution method for measuring an atrial septal defect shunt size
por: Muroke, Valtteri, et al.
Publicado: (2020) -
Mitochondrial disorders and ASD. Mechanisms of mitochondrial dysfunction in ASD
por: Sidenkova, A.
Publicado: (2023) -
Clinical phenotype of ASD-associated DYRK1A haploinsufficiency
por: Earl, Rachel K., et al.
Publicado: (2017) -
Visual search in ADHD, ASD and ASD + ADHD: overlapping or dissociating disorders?
por: Seernani, D., et al.
Publicado: (2020)