Your browser doesn't support javascript.
loading
Skeletal dysplasias in Latin America.
Cavalcanti, Denise P; Fano, Virginia; Mellado, Cecilia; Lacarrubba-Flores, Maria Dora J; Silveira, Cynthia; Silveira, Karina C; Del Pino, Mariana; Moresco, Angelica; Caino, Silvia; Ramos Mejía, Rosario; García, Cristián J; Lay-Son, Guillermo; Ferreira, Carlos R.
Afiliação
  • Cavalcanti DP; Skeletal Dysplasia Group, Medical Genetics Department, Medical Sciences Faculty, State University of Campinas (UNICAMP), Campinas, São Paulo, Brazil.
  • Fano V; Growth and Development Department, Garrahan Hospital, Buenos Aires, Argentina.
  • Mellado C; Study Group of Genetic Skeletal Abnormalities, Genetic Unit, Pediatrics Division, Faculty of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Lacarrubba-Flores MDJ; Skeletal Dysplasia Group, Medical Genetics Department, Medical Sciences Faculty, State University of Campinas (UNICAMP), Campinas, São Paulo, Brazil.
  • Silveira C; Skeletal Dysplasia Group, Medical Genetics Department, Medical Sciences Faculty, State University of Campinas (UNICAMP), Campinas, São Paulo, Brazil.
  • Silveira KC; Skeletal Dysplasia Group, Medical Genetics Department, Medical Sciences Faculty, State University of Campinas (UNICAMP), Campinas, São Paulo, Brazil.
  • Del Pino M; Growth and Development Department, Garrahan Hospital, Buenos Aires, Argentina.
  • Moresco A; Genetic Department, Garrahan Hospital, Buenos Aires, Argentina.
  • Caino S; Growth and Development Department, Garrahan Hospital, Buenos Aires, Argentina.
  • Ramos Mejía R; Growth and Development Department, Garrahan Hospital, Buenos Aires, Argentina.
  • García CJ; Study Group of Genetic Skeletal Abnormalities, Department of Radiology, Faculty of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Lay-Son G; Study Group of Genetic Skeletal Abnormalities, Genetic Unit, Pediatrics Division, Faculty of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Ferreira CR; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Am J Med Genet C Semin Med Genet ; 184(4): 986-995, 2020 12.
Article em En | MEDLINE | ID: mdl-33219737
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteocondrodisplasias Tipo de estudo: Prevalence_studies / Risk_factors_studies Limite: Humans País/Região como assunto: America do sul / Argentina Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteocondrodisplasias Tipo de estudo: Prevalence_studies / Risk_factors_studies Limite: Humans País/Região como assunto: America do sul / Argentina Idioma: En Ano de publicação: 2020 Tipo de documento: Article