MeSH Browser

MeSH Supplementary: Dyserythropoiesis, Congenital, with Internuclear Chromatin Bridges and Ultrastructurally Normal Erythroblast Heterochromatin
Unique ID: C566368
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566368
Registry Number: 0
Heading Mapped to: Anemia / *congenital; Erythrocytes, Abnormal
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Dyserythropoiesis, Congenital, with Internuclear Chromatin Bridges and Ultrastructurally Normal Erythroblast Heterochromatin MeSH Supplementary Concept Data 2024