Familial inheritance of the 3q29 microdeletion syndrome: case report and review

BACKGROUND: The chromosome 3q29 microdeletion syndrome is characterized by a clinical phenotype that includes behavioral features consistent with autism and attention deficit hyperactivity disorder, mild to moderate developmental delay, language-based learning disabilities, and/or dysmorphic feature...

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Detalles Bibliográficos
Autores principales: Khan, Wahab A., Cohen, Ninette, Scott, Stuart A., Pereira, Elaine M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421695/
https://www.ncbi.nlm.nih.gov/pubmed/30885185
http://dx.doi.org/10.1186/s12920-019-0497-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421695/
https://www.ncbi.nlm.nih.gov/pubmed/30885185
http://dx.doi.org/10.1186/s12920-019-0497-4

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