Your browser doesn't support javascript.
loading
Pediatric myelofibrosis due to compound heterozygous MPIG6B mutations in a patient of European ancestry.
Yenwongfai, Leonard N; Arora, Ranjana; Smith, Alexander P; Kalfa, Theodosia; Husami, Ammar; Radulescu, Vlad; Myers, Kasiani; Lorsbach, Robert.
Afiliação
  • Yenwongfai LN; Department of Pathology and Laboratory Medicine, University of Kentucky College of Medicine, Lexington, Kentucky, USA.
  • Arora R; Department of Pathology and Laboratory Medicine, University of Kentucky College of Medicine, Lexington, Kentucky, USA.
  • Smith AP; Department of Pathology and Laboratory Medicine, University of Kentucky College of Medicine, Lexington, Kentucky, USA.
  • Kalfa T; Cincinnati Children's, Cincinnati, Ohio, USA.
  • Husami A; Cincinnati Children's, Cincinnati, Ohio, USA.
  • Radulescu V; Pediatric Hematology and Oncology, University of Kentucky College of Medicine, Lexington, Kentucky, USA.
  • Myers K; Cincinnati Children's, Cincinnati, Ohio, USA.
  • Lorsbach R; Cincinnati Children's, Cincinnati, Ohio, USA.
Pediatr Blood Cancer ; 70(3): e30023, 2023 03.
Article em En | MEDLINE | ID: mdl-36184776
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mielofibrose Primária Limite: Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mielofibrose Primária Limite: Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article