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Atypical Association of Angelman Syndrome and Klinefelter Syndrome in a Boy with 47,XXY Karyotype and Deletion 15q11.2-q13.
Sánchez, Javier; Peciña, Ana; Alonso-Luengo, Olga; González-Meneses, Antonio; Vázquez, Rocío; Antiñolo, Guillermo; Borrego, Salud.
Afiliación
  • Sánchez J; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.
  • Peciña A; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain ; Centre of Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.
  • Alonso-Luengo O; Department of Pediatrics, University Hospital Virgen del Rocío, Avenida Manuel Siurot s/n, 41013 Seville, Spain.
  • González-Meneses A; Department of Pediatrics, University Hospital Virgen del Rocío, Avenida Manuel Siurot s/n, 41013 Seville, Spain.
  • Vázquez R; Department of Neurophysiology, University Hospital Virgen del Rocío, Avenida Manuel Siurot s/n, 41013 Seville, Spain.
  • Antiñolo G; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain ; Centre of Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.
  • Borrego S; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain ; Centre of Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.
Case Rep Genet ; 2014: 517091, 2014.
Article en En | MEDLINE | ID: mdl-25379297
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Texto completo: 1 Colección: 01-internacional Tipo de estudio: Guideline / Prognostic_studies / Risk_factors_studies / Screening_studies Idioma: En Revista: Case Rep Genet Año: 2014 Tipo del documento: Article País de afiliación: España
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Tipo de estudio: Guideline / Prognostic_studies / Risk_factors_studies / Screening_studies Idioma: En Revista: Case Rep Genet Año: 2014 Tipo del documento: Article País de afiliación: España