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Clinical and Genetic Aspects of Phelan-McDermid Syndrome: An Interdisciplinary Approach to Management.
Cammarata-Scalisi, Francisco; Callea, Michele; Martinelli, Diego; Willoughby, Colin Eric; Tadich, Antonio Cárdenas; Araya Castillo, Maykol; Lacruz-Rengel, María Angelina; Medina, Marco; Grimaldi, Piercesare; Bertini, Enrico; Nevado, Julián.
Afiliación
  • Cammarata-Scalisi F; Pediatric Service, Regional of Antofagasta Hospital, Antofagasta 1240835, Chile.
  • Callea M; Pediatric Dentistry and Special Dental Care Unit, Meyer Children's University Hospital, 50139 Florence, Italy.
  • Martinelli D; Unit of Metabolism, Bambino Gesù Children's Research Hospital IRCCS, 00165 Rome, Italy.
  • Willoughby CE; Genomic Medicine, Biomedical Sciences Research Institute, Ulster University, Coleraine Campus, Coleraine BT52 1SA, Northern Ireland, UK.
  • Tadich AC; Pediatric Service, Regional of Antofagasta Hospital, Antofagasta 1240835, Chile.
  • Araya Castillo M; Clinical Laboratory, Regional of Antofagasta Hospital, Antofagasta 1240835, Chile.
  • Lacruz-Rengel MA; Neuropediatrics Service, Childcare and Pediatric Department, University of Los Andes, Mérida 51101, Venezuela.
  • Medina M; Pediatric Service, Regional of Antofagasta Hospital, Antofagasta 1240835, Chile.
  • Grimaldi P; Department of Public Health and Pediatric Sciences, University of Torino, 10126 Torino, Italy.
  • Bertini E; Unit of Neuromuscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, Department of Neurosciences, Bambino Gesu' Children's Research Hospital IRCCS, 00165 Rome, Italy.
  • Nevado J; Instituto de Genética Médica y Molecular (INGEMM), Instituto de Investigación del Hospital Universitario La Paz (IdIPaz), 28046 Madrid, Spain.
Genes (Basel) ; 13(3)2022 03 12.
Article en En | MEDLINE | ID: mdl-35328058
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastornos de los Cromosomas / Trastorno del Espectro Autista Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Chile
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastornos de los Cromosomas / Trastorno del Espectro Autista Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Chile