1. A 69‐year‐old woman with Coffin–Siris syndrome. Issue 8 (28th July 2018) Authors: Määttänen, Laura; Hietala, Marja; Ignatius, Jaakko; Arvio, Maria Journal: American journal of medical genetics Issue: Volume 176:Issue 8(2018) Page Start: 1764 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Adult phenotype of the homozygous missense mutation c.655G>A, p.Gly219Arg in SLC13A5: A case report. Issue 11 (17th August 2020) Authors: Arvio, Maria; Lähdetie, Jaana Journal: American journal of medical genetics Issue: Volume 182:Issue 11(2020) Page Start: 2671 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Age at Death in Individuals with Intellectual Disabilities. Issue 4 (1st July 2016) Authors: Arvio, Maria; Salokivi, Tommi; Bjelogrlic‐Laakso, Nina Journal: Journal of applied research in intellectual disabilities Issue: Volume 30:Issue 4(2017:Jul.) Page Start: 782 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Ageing and cognition in men with fragile X syndrome. Issue 5 (12th April 2020) Authors: Sauna‐aho, Oili; Bjelogrlic‐Laakso, Nina; Rautava, Päivi; Arvio, Maria Journal: Journal of applied research in intellectual disabilities Issue: Volume 33:Issue 5(2020:Sep.) Page Start: 1113 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Aspartylglycosaminuria: a review. Issue 1 (December 2016) Authors: Arvio, Maria; Mononen, Ilkka Journal: Orphanet journal of rare diseases Issue: Volume 11:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Cognition in adults with Williams syndrome—A 20‐year follow‐up study. Issue 6 (29th April 2019) Authors: Sauna‐aho, Oili; Bjelogrlic‐Laakso, Nina; Sirén, Auli; Kangasmäki, Virpi; Arvio, Maria Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 6(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Intellectual disability in patients with epilepsy with eyelid myoclonias. (18th May 2018) Authors: Arvio, Maria; Sauna-aho, Oili; Nyrke, Timo; Bjelogrlic-Laakso, Nina Journal: SAGE open medical case reports Issue: Volume 6(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Manifestations of Intellectual Disability, Dystonia, and Parkinson's Disease in an Adult Patient with ARX Gene Mutation c.558_560dup p.(Pro187dup). (9th February 2023) Authors: Arvio, Maria; Lähdetie, Jaana; Koivu, Hannu; Sohlberg, Antti; Pekkonen, Eero Other Names: Mittal Balraj Academic Editor. Journal: Case reports in genetics Issue: Volume 2023(2023) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Mortality in individuals with intellectual disabilities in Finland. Issue 2 (24th January 2016) Authors: Arvio, Maria; Salokivi, Tommi; Tiitinen, Aila; Haataja, Leena Journal: Brain and behavior Issue: Volume 6:Issue 2(2016) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Natural history of alpha‐thalassemia X‐linked intellectual disability syndrome: A case report of a 45‐year‐old man. Issue 7 (4th May 2021) Authors: Arvio, Maria; Lähdetie, Jaana Journal: American journal of medical genetics Issue: Volume 185:Issue 7(2021) Page Start: 2164 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗