Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias

Author:

Russo Roberta12ORCID,Andolfo Immacolata12ORCID,Manna Francesco12,Gambale Antonella12,Marra Roberta12,Rosato Barbara Eleni12,Caforio Paola12,Pinto Valeria3,Pignataro Piero2,Radhakrishnan Kottayam45,Unal Sule6,Tomaiuolo Giovanna7,Forni Gian Luca3ORCID,Iolascon Achille12

Affiliation:

1. Dipartimento di Medicina Molecolare e Biotecnologie Mediche; Università degli Studi di Napoli Federico II; Napoli Italy

2. CEINGE Biotecnologie Avanzate; Napoli Italy

3. Centro della Microcitemia e Anemie Congenite, Ospedale Galliera; Genova Italy

4. Paediatric Haematology/Oncology, Children's Cancer Centre, Monash Children's Hospital; Melbourne Victoria 3168 Australia

5. Department of Haematology; Monash Medical Centre; Melbourne Victoria 3168 Australia

6. Division of Pediatric Hematology; Hacettepe University; Ankara Turkey

7. Dipartimento di Ingegneria Chimica; dei Materiali e della Prod. Indus., Federico II; Napoli Italy

Funder

Italian Ministry of University and Research, by PRIN

Regione Campania

Publisher

Wiley

Subject

Hematology

Reference28 articles.

1. Diagnosis and management of congenital dyserythropoietic anemias;Gambale;Expert Rev Hematol.,2016

2. Molecular approaches to diagnose Diamond-Blackfan anemia: the EuroDBA experience;Da Costa;Eur J Med Genet.,2017

3. New insights on hereditary erythrocyte membrane defects;Andolfo;Haematologica.,2016

4. Hereditary stomatocytosis: an underdiagnosed condition;Andolfo;Am J Hematol.,2018

5. Glucose-6-phosphate dehydrogenase deficiency;Luzzatto;Hematol Oncol Clin North Am.,2016

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