The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper-Reference-Cited by-同舟云学术

The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper

Published:2022-06 Issue:6 Volume:6 Page:e739
ISSN:2572-9241
Container-title:HemaSphere
language:en
Short-container-title:

Author:

Roy Noémi B. A.,Da Costa Lydie,Russo Roberta,Bianchi Paola,del Mar Mañú-Pereira Maria,Fermo Elisa,Andolfo Immacolata,Clark Barnaby,Proven Melanie,Sanchez Mayka,van Wijk Richard,van der Zwaag Bert,Layton Mark,Rees David,Iolascon Achille,

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology

Reference25 articles.

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2. Clinical utility of next-generation sequencing in the diagnosis of hereditary haemolytic anaemias.;Agarwal;Br J Haematol,2016

3. A novel PKLR gene mutation identified using advanced molecular techniques.;He;Pediatr Transplant,2018

4. Novel and known ribosomal causes of Diamond-Blackfan anaemia identified through comprehensive genomic characterisation.;Mirabello;J Med Genet,2017

5. Whole-exome analysis to detect congenital hemolytic anemia mimicking congenital dyserythropoietic anemia.;Hamada;Int J Hematol,2018

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