HEMPAS

Author:

Fukuda Michiko N

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference55 articles.

1. Familial erythroid multinuclearity;Wolff;Blood,1951

2. Congenital dyserythropoietic anemia with karyorrhexis and multinuclearity of erythroblasts;Heimpel;Helv. Med. Acta,1968

3. Hereditary erythroblastic multinuclearity associated with a positive acidified serum test; a typical congenital dyserythropoietic anemia;Crookston;Br. J. Haematol.,1969

4. HEMPAS: Congenital dyserythropoietic anemia (type II);Verwilghen;Q. J. Med. New Series,1973

5. Electron microscopy in the diagnosis of the bonemarrow disorders of the erythroid series;Fresco;Semin. Hematol.,1981

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1. New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II;International Journal of Molecular Sciences;2023-06-09

2. Inherited Bone Marrow Failure Syndromes;Anemia in the Young and Old;2018-11-14

3. Bone marrow failure syndromes, a practical approach to diagnosis;Journal of Hematopathology;2015-08-06

4. Mannosidase, Alpha, Class 2a1 (MAN2A1, Golgi α-Mannosidase II);Handbook of Glycosyltransferases and Related Genes;2014

5. The molecular biology of blood groups;ISBT Science Series;2009-11

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