Editorial: Towards a European consensus guideline for Phelan-McDermid syndrome.

van Ravenswaaij-Arts, Conny M A; van Balkom, Ingrid D C; Jesse, Sarah; Bonaglia, Maria C

van Ravenswaaij-Arts, Conny M A; van Balkom, Ingrid D C; Jesse, Sarah; Bonaglia, Maria C.

Afiliação

van Ravenswaaij-Arts CMA; University of Groningen, University Medical Centre Groningen, Dept. Genetics, Groningen, Netherlands; Autism Team Northern-Netherlands/Jonx, Department of (Youth) Mental Health and Autism, Lentis Psychiatric Institute, Groningen, the Netherlands. Electronic address: c.m.a.van.ravenswaaij@umcg.nl.
van Balkom IDC; Autism Team Northern-Netherlands/Jonx, Department of (Youth) Mental Health and Autism, Lentis Psychiatric Institute, Groningen, the Netherlands; Rob Giel Research Centre, Department of Psychiatry, University Medical Centre Groningen, Groningen, Netherlands.
Jesse S; University of Ulm, Department of Neurology, Ulm, Germany.
Bonaglia MC; Cytogenetics Laboratory, Scientific Institute, IRCCS Eugenio Medea, Bosisio Parini, Lecco, Italy.

Eur J Med Genet ; 66(5): 104736, 2023 05.

Article em En | MEDLINE | ID: mdl-36907549

Assuntos

Transtornos Cromossômicos; Humanos; Transtornos Cromossômicos/diagnóstico; Transtornos Cromossômicos/genética; Deleção Cromossômica; Cromossomos Humanos Par 22/genética

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Cromossômicos Tipo de estudo: Diagnostic_studies / Guideline Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google