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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.
Afiliación
  • 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 en En | MEDLINE | ID: mdl-36803953
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neurofibromatosis 1 / Neurofibromatosis / Síndrome de Noonan Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Child / Female / Humans País/Región como asunto: Asia Idioma: En Revista: Hum Genomics Asunto de la revista: GENETICA Año: 2023 Tipo del documento: Article País de afiliación: Irán
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neurofibromatosis 1 / Neurofibromatosis / Síndrome de Noonan Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Child / Female / Humans País/Región como asunto: Asia Idioma: En Revista: Hum Genomics Asunto de la revista: GENETICA Año: 2023 Tipo del documento: Article País de afiliación: Irán