An unusual case of non secretory multiple myeloma with intracellular lambda chains

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Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies.

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Diagnostic application of a capture based NGS test for the concurrent detection of variants in sequence and copy number as well as LOH.

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von Willebrand disease type 1 mutation p.Arg1379Cys and the variant p.Ala1377Val synergistically determine a 2M phenotype in four Italian patients.

Haemophilia : the official journal of the World Federation of Hemophilia·2016

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Revista iberoamericana de micologia·2026

Diagnostic Yield and Cost of Morphology-Guided Immunohistochemistry in Liver Tumors.

Asian Pacific journal of cancer prevention : APJCP·2026

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Frontiers in cellular and infection microbiology·2026

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Journal of immunology research·2026

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The Journal of international medical research·2026

Serological Detection of Antibodies Against Mycoplasma bovis Infection by Competitive Enzyme-Linked Immunosorbent Assay (cELISA).

Veterinary sciences·2026

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An unusual case of non secretory multiple myeloma with intracellular lambda chains

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