Clinical heterogeneity in a family with <i>DKC1</i> mutation, dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome in first cousins.

Clinical heterogeneity in a family with DKC1 mutation, dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome in first cousins.

Olivieri, Cristina; Mondino, Anna; Chinello, Matteo; Risso, Alessandra; Finale, Enrico; Lanciotti, Marina; Guala, Andrea.

Afiliação

Olivieri C; Department of Public and Pediatric Health Sciences, University of Turin.
Mondino A; Department of Public and Pediatric Health Sciences, University of Turin.
Chinello M; Department of Pediatric Hematology and Oncology, Policlinico G.B. Rossi, Verona.
Risso A; Departement of Hematology, City of Health and Science, University of Turin.
Finale E; Unit of Pediatrics, Castelli Hospital, Verbania.
Lanciotti M; Department of Pediatric Hematology Oncology and Bone Marrow Transplant, G. Gaslini Children's Hospital, Genoa, Italy.
Guala A; Unit of Pediatrics, Castelli Hospital, Verbania.

Pediatr Rep ; 9(3): 7301, 2017 Oct 06.

Article em En | MEDLINE | ID: mdl-29081935