Your browser doesn't support javascript.
loading
Neurofibromatosis-Noonan syndrome and growth deficiency in an Iranian girl due to a pathogenic variant in NF1 gene.
Dalili, Setila; Hoseini Nouri, Seyyedeh Azade; Bayat, Reza; Koohmanaee, Shahin; Tabrizi, Manijeh; Zarkesh, Marjaneh; Tarang, Alireza; Mahdieh, Nejat.
Afiliação
  • Dalili S; Pediatric Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran.
  • Hoseini Nouri SA; Pediatric Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran. dr.azadehoseini@gmail.com.
  • Bayat R; Pediatric Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran.
  • Koohmanaee S; Pediatric Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran.
  • Tabrizi M; Pediatric Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran.
  • Zarkesh M; Pediatric Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran.
  • Tarang A; Agriculture Biotechnology Research Institute, Agricultural Research, Education and Extension Organization (AREEO), Rasht, Iran.
  • Mahdieh N; Growth and Development Research Center, Tehran University of Medical Sciences, Tehran, Iran. nmahdieh@yahoo.com.
Hum Genomics ; 17(1): 12, 2023 02 20.
Article em En | MEDLINE | ID: mdl-36803953
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neurofibromatose 1 / Neurofibromatoses / Síndrome de Noonan Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child / Female / Humans País/Região como assunto: Asia Idioma: En Revista: Hum Genomics Assunto da revista: GENETICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Irã
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neurofibromatose 1 / Neurofibromatoses / Síndrome de Noonan Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child / Female / Humans País/Região como assunto: Asia Idioma: En Revista: Hum Genomics Assunto da revista: GENETICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Irã