Robertsonian translocation between the chromosome Y and 15

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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.

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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

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Humangenetik·1975

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

Humangenetik·1975

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Lithopedion in a 70-year-old woman: incidental finding in the greater omentum.

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Stillbirths Occur in the U.S. More Often Than Reported.

The American journal of nursing·2026

Constant ovulation during oral contraceptive treatment: Follicle-stimulating hormone-secreting pituitary adenoma case report and literature review.

Journal of family medicine and primary care·2026

Huge retroperitoneal leiomyoma: a case report of a massive 35 cm tumor presenting with vague abdominal pain.

International journal of surgery case reports·2026

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Robertsonian translocation between the chromosome Y and 15

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Reporting framework in the testing of predisposition to common adult solid tumors using next-generation sequencing.

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).

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

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

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Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

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Robertsonian translocation between the chromosome Y and 15

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