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Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature.
Béna F, Bruno DL, Eriksson M, van Ravenswaaij-Arts C, Stark Z, Dijkhuizen T, Gerkes E, Gimelli S, Ganesamoorthy D, Thuresson AC, Labalme A, Till M, Bilan F, Pasquier L, Kitzis A, Dubourgm C, Rossi M, Bottani A, Gagnebin M, Sanlaville D, Gilbert-Dussardier B, Guipponi M, van Haeringen A, Kriek M, Ruivenkamp C, Antonarakis SE, Anderlid BM, Slater HR, Schoumans J. Béna F, et al. Among authors: eriksson m. Am J Med Genet B Neuropsychiatr Genet. 2013 Jun;162B(4):388-403. doi: 10.1002/ajmg.b.32148. Epub 2013 Mar 26. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23533028 Review.
Copy number variation characteristics in subpopulations of patients with autism spectrum disorders.
Bremer A, Giacobini M, Eriksson M, Gustavsson P, Nordin V, Fernell E, Gillberg C, Nordgren A, Uppströmer A, Anderlid BM, Nordenskjöld M, Schoumans J. Bremer A, et al. Among authors: eriksson m. Am J Med Genet B Neuropsychiatr Genet. 2011 Mar;156(2):115-24. doi: 10.1002/ajmg.b.31142. Epub 2010 Dec 8. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21302340
Morbidity and mortality among children, adolescents, and young adults with cancer over six decades: a Swedish population-based cohort study (the Rebuc study).
Stenmarker M, Mallios P, Hedayati E, Rodriguez-Wallberg KA, Johnsson A, Alfredsson J, Ekman B, Legert KG, Borland M, Mellergård J, Eriksson M, Marteinsdottir I, Davidson T, Engerström L, Sandsveden M, Keskisärkkä R, Singull M, Hubbert L. Stenmarker M, et al. Among authors: eriksson m. Lancet Reg Health Eur. 2024 May 15;42:100925. doi: 10.1016/j.lanepe.2024.100925. eCollection 2024 Jul. Lancet Reg Health Eur. 2024. PMID: 38800108 Free PMC article.
2,036 results