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Publikováno v:
Molecular Syndromology. 8:219-223
The Xp22.31 duplication is a copy number variant which is challenging to categorize as pathogenic or benign. There is an increasing number of patients with the duplication and a neurobehavioral phenotype, but the duplication is almost always inherite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b8e2382047e90b18ada86c24f95ca53
https://doi.org/10.1159/000475795
https://doi.org/10.1159/000475795
