Phenotype variability in thirteen 16p11.2 deletion patients

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Bibliographic Details
Published in:Anales de Pediatría 2018-07, Vol.89 (1), p.62-63
Main Authors: Rodà, Diana, Gabau, Elisabeth, Baena, Neus, Guitart, Miriam
Format: Article
Language:Spanish
Subjects:
Adolescent
Adult
Autistic Disorder - genetics
Child
Chromosome Deletion
Chromosome Disorders - genetics
Chromosomes, Human, Pair 16 - genetics
Female
Humans
Intellectual Disability - genetics
Male
Phenotype
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ISSN:2341-2879
2341-2879
DOI:10.1016/j.anpedi.2017.08.003