Complex genomic alterations and intellectual disability: an interpretative challenge.

Silipigni, R; Milani, D; Tolva, G; Monfrini, E; Giacobbe, A; Marchisio, P G; Guerneri, S

Silipigni, R; Milani, D; Tolva, G; Monfrini, E; Giacobbe, A; Marchisio, P G; Guerneri, S.

Afiliación

Silipigni R; Laboratory of Medical Genetics, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Milani D; Pediatric Highly Intensive Care Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Tolva G; Pediatric Highly Intensive Care Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Monfrini E; Neurology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Giacobbe A; Dino Ferrari Center, Neuroscience Section, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.
Marchisio PG; Child and Adolescent Neuropsychiatric Service (UONPIA), Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Guerneri S; Pediatric Highly Intensive Care Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

J Intellect Disabil Res ; 65(2): 113-124, 2021 02.

Article en En | MEDLINE | ID: mdl-33140510

Asunto(s)

Discapacidad Intelectual; Preescolar; Aberraciones Cromosómicas; Hibridación Genómica Comparativa; Genómica; Humanos; Hibridación Fluorescente in Situ; Discapacidad Intelectual/genética; Masculino

Palabras clave

aCGH; complex chromosomal rearrangements; congenital abnormalities; developmental delay; insertional translocation; non-contiguous gains

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Discapacidad Intelectual Límite: Child, preschool / Humans / Male Idioma: En Revista: J Intellect Disabil Res Asunto de la revista: TRANSTORNOS MENTAIS Año: 2021 Tipo del documento: Article País de afiliación: Italia

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google