Identification of microduplications at Xp21.2 and Xq13.1 in neurodevelopmental disorders

Kokkonen, H., Siren, A., Määttä, T., Kamila Kadlubowska, M., Acharya, A., Nouel‐Saied, L. M., Leal, S. M., Järvelä, I., & Schrauwen, I. (2021). Identification of microduplications at Xp21.2 and Xq13.1 in neurodevelopmental disorders. Molecular Genetics & Genomic Medicine, 9(12). Portico. https://doi.org/10.1002/mgg3.1703
Authors:
Hannaleena Kokkonen
Auli Siren
Tuomo Määttä
Magda Kamila Kadlubowska
Anushree Acharya
Liz M. Nouel-Saied
Suzanne M. Leal
Irma Järvelä
Isabelle Schrauwen
Affiliated Authors:
Magda Kamila Kadlubowska
Anushree Acharya
Liz M. Nouel-Saied
Suzanne M. Leal
Isabelle Schrauwen
Columbia Affiliation:
Author Keywords:
exome sequencing
intellectual disability
microduplication
neurodevelopmental disorders
x-chromosome
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Publication Type:
Article
Unique ID:
10.1002/mgg3.1703
PMID:
33982443
DOI:
10.1002/mgg3.1703
Journal:
Molecular Genetics and Genomic Medicine
Publication Date:
Data Source:
Scopus
Source Link:
View Scopus Record

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