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Clinical Profile of Ghosal Hematodiaphyseal Dysplasia Presenting as Bone Marrow FailureDOI 10.1007/s12288-026-02526-0
Ghosal Type Hematodiaphyseal Dysplasia- A rare and unusual cause of cytopeniasSemantic proximity
Pathophysiology and management of inherited bone marrow failure syndromesSemantic proximity
Ghosal Hematodiaphyseal Dysplasia: A Case Report With Review of Genetically Confirmed Cases.Semantic proximity
The Inherited Bone Marrow Failure SyndromesSemantic proximity
Acquired and germline predisposition to bone marrow failure: Diagnostic features and clinical implicationsSemantic proximity
Inherited bone marrow failure syndromesSemantic proximity
Minimal morphological criteria for defining bone marrow dysplasia: a basis for clinical implementation of WHO classification of myelodysplastic syndromesSemantic proximity
Genomic Characterization of the Inherited Bone Marrow Failure SyndromesSemantic proximity
Clonal hematopoiesis and bone marrow failure syndromesSemantic proximity
Hypophosphatasia diagnosis: current state of the art and proposed diagnostic criteria for children and adults.Semantic proximity
Neonatal manifestations of inherited bone marrow failure syndromesSemantic proximity
The skeletal manifestations of the congenital disorders of glycosylation.Semantic proximity
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