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The guidelines for clinical practice for carriers of germline mutations in hereditary breast, ovarian, prostate, and pancreatic cancer predisposition genes BRCA1, BRCA2, PALB2, ATM, and CHEK2 (4.2024).

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Precise determination of primary cytogenetic abnormalities provides added value for stratification of chronic lymphocytic leukemia patients.

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Allogeneic stem cell transplantation can improve outcome of AML patients without complete cytogenetic response after induction and consolidation treatment.

Neoplasma·2015

The association of factor V Leiden with various clinical patterns of venous thromboembolism-the factor V Leiden paradox.

QJM : monthly journal of the Association of Physicians·2014

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Humangenetik·1975

Climate associated variations in the human serum albumin level.

Humangenetik·1975

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Humangenetik·1975

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Humangenetik·1975

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Humangenetik·1975

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Humangenetik·1975

MIT/TFE family transcription factors, Mitf and Tfec, redundantly promote pigment cell differentiation and retinal epithelium pigmentation in teleosts.

Developmental dynamics : an official publication of the American Association of Anatomists·2026

Electromagnetic radiation induced by proton interaction with aluminum nanosheets.

Physical chemistry chemical physics : PCCP·2026

Observation of a relativistic analog of the Brewster effect in electron-photon scattering.

Nature communications·2026

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Molecular biology reports·2026

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Sensors (Basel, Switzerland)·2026

Keratinocytes with DNA Aberration Induced by UVB Become Susceptible to Ferroptosis.

Antioxidants (Basel, Switzerland)·2026

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The guidelines for clinical practice for carriers of germline mutations in the Lynch syndrome predisposition genes MLH1, MSH2, MSH6, PMS2 and large deletions of EPCAM (4.2024).

The guidelines for clinical practice for carriers of germline mutations in hereditary breast, ovarian, prostate, and pancreatic cancer predisposition genes BRCA1, BRCA2, PALB2, ATM, and CHEK2 (4.2024).

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