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Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population

Detalles Bibliográficos
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
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author Muroke, Valtteri
Jalanko, Mikko
Ruotsalainen, Sanni
Perola, Markus
Helle, Emmi
Sinisalo, Juha
author_facet Muroke, Valtteri
Jalanko, Mikko
Ruotsalainen, Sanni
Perola, Markus
Helle, Emmi
Sinisalo, Juha
author_sort Muroke, Valtteri
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spelling pubmed-105814112023-10-18 Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population Muroke, Valtteri Jalanko, Mikko Ruotsalainen, Sanni Perola, Markus Helle, Emmi Sinisalo, Juha Circ Genom Precis Med Research Letters Lippincott Williams & Wilkins 2023-08-14 /pmc/articles/PMC10581411/ /pubmed/37577800 http://dx.doi.org/10.1161/CIRCGEN.123.004070 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Circulation: Genomic and Precision Medicine is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited.
spellingShingle Research Letters
Muroke, Valtteri
Jalanko, Mikko
Ruotsalainen, Sanni
Perola, Markus
Helle, Emmi
Sinisalo, Juha
Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population
title Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population
title_full Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population
title_fullStr Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population
title_full_unstemmed Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population
title_short Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population
title_sort phenotype of asds associated with 4p16 risk locus and novel genome-wide associations of asd patients in the finnish population
topic Research Letters
url 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
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