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Clinical and cytogenomic findings in OAV spectrum.
Bragagnolo, Silvia; Colovati, Mileny E S; Souza, Malu Z; Dantas, Anelise G; F de Soares, Maria F; Melaragno, Maria I; Perez, Ana B.
Afiliación
  • Bragagnolo S; Department of Morphology and Genetics, Federal University of São Paulo, São Paulo, Brazil.
  • Colovati MES; Department of Morphology and Genetics, Federal University of São Paulo, São Paulo, Brazil.
  • Souza MZ; Department of Morphology and Genetics, Federal University of São Paulo, São Paulo, Brazil.
  • Dantas AG; Department of Morphology and Genetics, Federal University of São Paulo, São Paulo, Brazil.
  • F de Soares MF; Department of Radiology, Federal University of São Paulo, São Paulo, Brazil.
  • Melaragno MI; Department of Morphology and Genetics, Federal University of São Paulo, São Paulo, Brazil.
  • Perez AB; Department of Morphology and Genetics, Federal University of São Paulo, São Paulo, Brazil.
Am J Med Genet A ; 176(3): 638-648, 2018 03.
Article en En | MEDLINE | ID: mdl-29368383

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Aberraciones Cromosómicas / Estudios de Asociación Genética / Síndrome de Goldenhar Tipo de estudio: Diagnostic_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Aberraciones Cromosómicas / Estudios de Asociación Genética / Síndrome de Goldenhar Tipo de estudio: Diagnostic_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Estados Unidos