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A 3-Year-Old Boy with an Xp21 Deletion Syndrome: A Case Report.
Sadeghmousavi, Shaghayegh; Shahkarami, Sepideh; Rayzan, Elham; Ahmed, Souran; Gharalari, Farzaneh Hosseini; Rohlfs, Meino; Klein, Christoph; Rezaei, Nima.
Afiliação
  • Sadeghmousavi S; School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Shahkarami S; Medical Genetics Network (MeGeNe), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
  • Rayzan E; Department of Pediatrics, Dr. von Hauner Children\'s Hospital, University Hospital, Ludwig-Maximilians-Universität München (LMU), Munich, Germany.
  • Ahmed S; Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
  • Gharalari FH; Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
  • Rohlfs M; International Hematology/Oncology of Pediatric Experts (IHOPE), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
  • Klein C; Kurdistan Pediatric Society, Department of Medicine, University of Sulaimani, Sulaimani, Iraq.
  • Rezaei N; Department of Pathology, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Endocr Metab Immune Disord Drug Targets ; 22(8): 881-887, 2022.
Article em En | MEDLINE | ID: mdl-35105298
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Adrenal / Distrofia Muscular de Duchenne Limite: Child, preschool / Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Adrenal / Distrofia Muscular de Duchenne Limite: Child, preschool / Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article