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Neuropsychiatric phenotype in relation to gene variants in the hemizygous allele in 3q29 deletion carriers: A case series
BACKGROUND: Genetic risk variants in the hemizygous allele may influence neuropsychiatric manifestations and clinical course in 3q29 deletion carriers. METHODS: In‐depth phenotypic assessment in two deletion carriers included medical records, medical, genetic, psychiatric and neuropsychological eval...
Autores principales: | Malt, Eva Albertsen, Juhasz, Katalin, Frengen, Anna, Wangensteen, Teresia, Emilsen, Nina Merete, Hansen, Borre, Agafonov, Oleg, Nilsen, Hilde Loge |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732294/ https://www.ncbi.nlm.nih.gov/pubmed/31347308 http://dx.doi.org/10.1002/mgg3.889 |
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