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Mosaic trisomy 22 in a 4-year-old boy with congenital heart disease and general hypotrophy: A case report.
Kalayinia, Samira; Shahani, Tina; Biglari, Alireza; Maleki, Majid; Rokni-Zadeh, Hassan; Razavi, Zahra; Mahdieh, Nejat.
  • Kalayinia S; Department of Genetics and Molecular Medicine, School of Medicine, Zanjan University of Medical Sciences (ZUMS), Zanjan, Iran.
  • Shahani T; Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.
  • Biglari A; Department of Genetics and Molecular Medicine, School of Medicine, Zanjan University of Medical Sciences (ZUMS), Zanjan, Iran.
  • Maleki M; Department of Genetics and Molecular Medicine, School of Medicine, Zanjan University of Medical Sciences (ZUMS), Zanjan, Iran.
  • Rokni-Zadeh H; Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.
  • Razavi Z; Department of Medical Biotechnology and Nanotechnology, School of Medicine, Zanjan University of Medical Sciences (ZUMS), Zanjan, Iran.
  • Mahdieh N; Pediatric Endocrinologist, Pediatrics Department, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
J Clin Lab Anal ; 33(2): e22663, 2019 Feb.
Article en En | MEDLINE | ID: mdl-30259573
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trisomía / Trastornos de los Cromosomas / Disomía Uniparental / Defectos del Tabique Interatrial Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Child, preschool / Humans / Male Idioma: En Año: 2019 Tipo del documento: Article
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trisomía / Trastornos de los Cromosomas / Disomía Uniparental / Defectos del Tabique Interatrial Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Child, preschool / Humans / Male Idioma: En Año: 2019 Tipo del documento: Article