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Publications by Barbara Bain
Congenital Dyserythropoietic Anemia Type 1: A Case With Novel Compound Heterozygous Mutations in the C15orf41 Gene
American Journal of Hematology
Hematology
A European Consensus Report on Blood Cell Identification: Terminology Utilized and Morphological Diagnosis Concordance Among 28 Experts From 17 Countries Within the European LeukemiaNet Network WP10, on Behalf of the ELN Morphology Faculty
British Journal of Haematology
Hematology
Related publications
Codanin-1 Mutations in Congenital Dyserythropoietic Anemia Type 1 Affect HP1 Localization in Erythroblasts
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Congenital Dyserythropoietic Anemia Type III
Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene
Turkish Journal of Haematology
Hematology
Characterization of the Interactions Between Codanin-1 and C15Orf41, Two Proteins Implicated in Congenital Dyserythropoietic Anemia Type I Disease
BMC Molecular and Cell Biology
Cell Biology
Molecular Biology
Thrombocytopenia With Congenital Dyserythropoietic Anemia
Novel Compound Heterozygous COG5 Mutations in a Chinese Male Patient With Severe Clinical Symptoms and Type�IIi Congenital Disorder of Glycosylation: A Case Report
Experimental and Therapeutic Medicine
Medicine
Cancer Research
Immunology
Microbiology
A Novel Compound Heterozygous Mutation of the AIRE Gene in a Patient With Autoimmune Polyendocrine Syndrome Type 1
Annals of Pediatric Endocrinology and Metabolism
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
A Case of Congenital Dyserythropoietic Anemia Type 1 in a Japanese Adult With a CDAN1 Gene Mutation and an Inappropriately Low Serum Hepcidin-25 Level
Internal Medicine
Internal Medicine
Medicine
Compound Heterozygous Novel Frameshift Variants in the PROM1 Gene Result in Leber Congenital Amaurosis
Cold Spring Harbor molecular case studies
Biochemistry
Molecular Medicine
Genetics
