Localization of the Congenital Dyserythropoietic Anemia II Locus to Chromosome 20q11.2 by Genomewide Search
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
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1. A case report of congenital dyserythropoietic anemia type II with a novel SEC23B mutation and accompanied by a large segmental deletion and literature review;2024-06-03
2. New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II;International Journal of Molecular Sciences;2023-06-09
3. Compound heterozygosity for two novel mutations of the SEC23B gene in congenital dyserythropoietic anemia type II;International Journal of Hematology;2021-04-29
4. Congenital Dyserythropoietic Anemia;Diagnostic Pathology: Blood and Bone Marrow;2018
5. Other Hereditary Red Blood Cell Disorders;Emery and Rimoin's Principles and Practice of Medical Genetics;2013
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