The Evolving Role of Next-Generation Sequencing in Screening and Diagnosis of Hemoglobinopathies.

Achour, Ahlem; Koopmann, Tamara T; Baas, Frank; Harteveld, Cornelis L

Achour, Ahlem; Koopmann, Tamara T; Baas, Frank; Harteveld, Cornelis L.

Afiliación

Achour A; Department of Clinical Genetics/LDGA, Leiden University Medical Center, Leiden, Netherlands.
Koopmann TT; Department of Congenital and Hereditary Diseases, Charles Nicolle Hospital, Tunis, Tunisia.
Baas F; Department of Clinical Genetics/LDGA, Leiden University Medical Center, Leiden, Netherlands.
Harteveld CL; Department of Clinical Genetics/LDGA, Leiden University Medical Center, Leiden, Netherlands.

Front Physiol ; 12: 686689, 2021.

Article en En | MEDLINE | ID: mdl-34385932

Palabras clave

NGS; WES; WGS; hemoglobinopathy diagnostics; sickle cell disease; α-thalassemia; ß-thalassemia

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Screening_studies Idioma: En Revista: Front Physiol Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google