Sonja Dahlum
Ulm, BW 89081, Germany
Last Updated: 09/26/2026
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Found 10 publications
Discrepant findings of prenatal diagnostics in a case of fetal partial trisomy 21 and fetoplacental mosaicism.
Journal: Molecular cytogenetics
Published: March 03, 2026
A rare case of atypical teratoid rhabdoid tumor (AT/RT) with homozygous SMARCB1 loss and one concurrent somatic heterozygous SMARCA4 variant.
Journal: Acta neuropathologica communications
Published: June 06, 2025
APC-related multiple salivary gland lesions: spatial transcriptomic analysis reveals progressive WNT activation.
Journal: The Journal of pathology
Published: April 29, 2025
Exploiting somatic oncogenic driver alterations in a patient with Li-Fraumeni syndrome- paving the path towards precision medicine: a case report.
Journal: Journal of cancer research and clinical oncology
Published: August 30, 2024
Desmoplastic Small Round Cell Tumors: Clinical Presentation, Molecular Characterization, and Therapeutic Approach of Seven Patients.
Journal: Sarcoma
Published: January 20, 2024
Lack of SMARCB1 expression characterizes a subset of human and murine peripheral T-cell lymphomas.
Journal: Nature communications
Published: May 04, 2023
Molecular characterization of an embryonal rhabdomyosarcoma occurring in a patient with Kabuki syndrome: report and literature review in the light of tumor predisposition syndromes.
Journal: Familial cancer
Published: May 04, 2022
SMARCB1-deficient and SMARCA4-deficient Malignant Brain Tumors With Complex Copy Number Alterations and TP53 Mutations May Represent the First Clinical Manifestation of Li-Fraumeni Syndrome.
Journal: The American journal of surgical pathology
Published: April 21, 2022
Showing 1-10 of 10
Last Updated: 09/26/2026