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Borderline cognitive level in a family with Bazex-Dupré-Christol syndrome.
Gonfiantini, Michaela Veronika; Armando, Marco; Pucciarini, Maria Laura; Macchiaiolo, Marina; Buonuomo, Paola Sabrina; Diociaiuti, Andrea; Lepri, Francesca Romana; Sirleto, Pietro; Vicari, Stefano; Bartuli, Andrea.
Afiliación
  • Gonfiantini MV; Department of Pediatric Medicine, Rare Diseases and Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Armando M; Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Pucciarini ML; Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Macchiaiolo M; Department of Human Sciences, Lumsa University, Rome, Italy.
  • Buonuomo PS; Department of Pediatric Medicine, Rare Diseases and Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Diociaiuti A; Department of Pediatric Medicine, Rare Diseases and Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Lepri FR; Dermatology, Department of Pediatric Medicine, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Sirleto P; Cytogenetics and Molecular Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Vicari S; Cytogenetics and Molecular Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Bartuli A; Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Am J Med Genet A ; 167(7): 1637-43, 2015 Jul.
Article en En | MEDLINE | ID: mdl-25820919
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Neoplasias Cutáneas / Carcinoma Basocelular / Trastornos del Conocimiento / Cabello / Hipotricosis Tipo de estudio: Prognostic_studies Límite: Adult / Child / Child, preschool / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
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XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Neoplasias Cutáneas / Carcinoma Basocelular / Trastornos del Conocimiento / Cabello / Hipotricosis Tipo de estudio: Prognostic_studies Límite: Adult / Child / Child, preschool / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Estados Unidos