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The Natural History of a Man With Ovotesticular 46,XX DSD Caused by a Novel 3-Mb 15q26.2 Deletion Containing NR2F2 Gene.
Carvalheira, Gianna; Malinverni, Andrea M; Moysés-Oliveira, Mariana; Ueta, Renata; Cardili, Leonardo; Monteagudo, Patrícia; Mathez, Andreia L G; Verreschi, Ieda T; Maluf, Miguel A; Shida, Márcia E F; Leite, Mila T C; Mazzotti, Diego; Melaragno, Maria Isabel; Dias-da-Silva, Magnus R.
Afiliación
  • Carvalheira G; Department of Morphology and Genetics, Division of Genetics, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.
  • Malinverni AM; Department of Morphology and Genetics, Division of Genetics, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.
  • Moysés-Oliveira M; Department of Pathology, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.
  • Ueta R; Department of Morphology and Genetics, Division of Genetics, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.
  • Cardili L; Department of Morphology and Genetics, Division of Genetics, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.
  • Monteagudo P; Department of Pathology, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.
  • Mathez ALG; Department of Medicine, Division of Endocrinology, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.
  • Verreschi IT; Department of Medicine, Division of Endocrinology, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.
  • Maluf MA; Department of Medicine, Division of Endocrinology, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.
  • Shida MEF; Department of Medicine, Division of Cardiovascular, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.
  • Leite MTC; Department of Medicine, Division of Pediatric Surgery, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.
  • Mazzotti D; Department of Medicine, Division of Pediatric Surgery, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.
  • Melaragno MI; Center for Sleep and Circadian Neurobiology, University of Pensylvania, Philadelphia, Pennsylvania.
  • Dias-da-Silva MR; Department of Morphology and Genetics, Division of Genetics, Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.
J Endocr Soc ; 3(11): 2107-2113, 2019 Nov 01.
Article en En | MEDLINE | ID: mdl-31687637
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Endocr Soc Año: 2019 Tipo del documento: Article País de afiliación: Brasil
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Endocr Soc Año: 2019 Tipo del documento: Article País de afiliación: Brasil