Your browser doesn't support javascript.
loading
Males with Paternally Inherited MKRN3 Mutations May Be Asymptomatic.
Dimitrova-Mladenova, Mihaela S; Stefanova, Elisaveta M; Glushkova, Maria; Todorova, Albena P; Todorov, Tihomir; Konstantinova, Maia M; Kazakova, Krasimira; Tincheva, Radka S.
Afiliação
  • Dimitrova-Mladenova MS; Department of Endocrinology and Genetics, University Children's Hospital, Medical University Sofia, Sofia, Bulgaria. Electronic address: mihaela_mail@abv.bg.
  • Stefanova EM; Department of Endocrinology and Genetics, University Children's Hospital, Medical University Sofia, Sofia, Bulgaria.
  • Glushkova M; Department of Medical Chemistry and Biochemistry, Medical University Sofia, Sofia, Bulgaria; Genetic Medico-Diagnostic Laboratory Genica, Sofia, Bulgaria.
  • Todorova AP; Department of Medical Chemistry and Biochemistry, Medical University Sofia, Sofia, Bulgaria; Genetic Medico-Diagnostic Laboratory Genica, Sofia, Bulgaria.
  • Todorov T; Genetic Medico-Diagnostic Laboratory Genica, Sofia, Bulgaria.
  • Konstantinova MM; Department of Endocrinology and Genetics, University Children's Hospital, Medical University Sofia, Sofia, Bulgaria.
  • Kazakova K; Department of Endocrinology and Genetics, University Children's Hospital, Medical University Sofia, Sofia, Bulgaria.
  • Tincheva RS; Department of Endocrinology and Genetics, University Children's Hospital, Medical University Sofia, Sofia, Bulgaria.
J Pediatr ; 179: 263-265, 2016 12.
Article em En | MEDLINE | ID: mdl-27640350
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Puberdade Precoce / Ribonucleoproteínas / Doenças Assintomáticas / Herança Paterna / Mutação Limite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: J Pediatr Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Puberdade Precoce / Ribonucleoproteínas / Doenças Assintomáticas / Herança Paterna / Mutação Limite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: J Pediatr Ano de publicação: 2016 Tipo de documento: Article