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Autism and intellectual disability in a patient with two microdeletions in 6q16: a contiguous gene deletion syndrome?
Strunk, Daniela; Weber, Peter; Röthlisberger, Benno; Filges, Isabel.
Afiliación
  • Strunk D; Medical Genetics, University Hospital Basel, Schönbeinstrasse 40, CH-4031 Basel, Switzerland.
  • Weber P; Division of Neuropediatrics and Developmental Pediatrics, University Children's Hospital, Spitalstrasse 33, CH-4056 Basel, Switzerland.
  • Röthlisberger B; Medical Genetics, Department of Laboratory Medicine, Cantonal Hospital Aarau, Tellstrasse, CH-5001 Aarau, Switzerland.
  • Filges I; Medical Genetics, University Hospital Basel and University of Basel, Schönbeinstrasse 40, CH-4031 Basel, Switzerland.
Mol Cytogenet ; 9: 88, 2016.
Article en En | MEDLINE | ID: mdl-27980676
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Mol Cytogenet Año: 2016 Tipo del documento: Article País de afiliación: Suiza
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Mol Cytogenet Año: 2016 Tipo del documento: Article País de afiliación: Suiza