A postulated mechanism for deletions with inversions

European LeukemiaNet-defined primary refractory acute myeloid leukemia: the value of allogeneic hematopoietic stem cell transplant and overall response.

Blood cancer journal·2022

Risk factors for arterial versus venous thrombosis in polycythemia vera: a single center experience in 587 patients.

Blood cancer journal·2017

Prognostic implications of abnormalities of chromosome 13 and the presence of multiple cytogenetic high-risk abnormalities in newly diagnosed multiple myeloma.

Blood cancer journal·2017

Prognostic relevance of lymphocytopenia, monocytopenia and lymphocyte-to-monocyte ratio in primary myelodysplastic syndromes: a single center experience in 889 patients.

Blood cancer journal·2017

Prognostic impact of bone marrow fibrosis in polycythemia vera: validation of the IWG-MRT study and additional observations.

Blood cancer journal·2017

Interphase fluorescence in situ hybridization in untreated AL amyloidosis has an independent prognostic impact by abnormality type and treatment category.

Leukemia·2016

Additive value of polygenic risk and family history for coronary heart disease risk stratification in two diverse US cohorts.

American journal of human genetics·2026

Landscape of parental postzygotic mutations across >11,000 rare disease trios.

American journal of human genetics·2026

Likelihood-based calibration improves the clinical utility of JAG1 functional data for variant classification.

American journal of human genetics·2026

Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorder.

American journal of human genetics·2026

Overlapping Xq13.3 duplications define an X-linked hypotrichosis simplex and implicate TAB3 dosage sensitivity.

American journal of human genetics·2026

Bi-allelic variants in CDK20 cause a severe ciliopathy with midline brain and facial anomalies.

American journal of human genetics·2026

Asymmetrical chromosomal utilization during zygotic genome activation.

Frontiers in bioinformatics·2026

DeepKaryo-Check: a two-stage automated screening framework for chromosomal numerical and structural abnormalities in clinical karyotype analysis.

Frontiers in cell and developmental biology·2026

Multiparametric analysis of sperm chromatin and ROS reveals the existence of subpopulations that are linked to embryo development after ICSI.

Scientific reports·2026

Repeat offenders: Satellite DNA sequence variation drives heterochromatin instability.

Science advances·2026

Nuclear Dynamics and Its Timing Regulation Revealed by Live-Cell Imaging.

Advances in experimental medicine and biology·2026

Oocyte Kinetochores at the Nexus of Meiotic Drive and Segregation Fidelity.

Advances in experimental medicine and biology·2026

Related Experiment Videos

A postulated mechanism for deletions with inversions

Related Concept Videos

European LeukemiaNet-defined primary refractory acute myeloid leukemia: the value of allogeneic hematopoietic stem cell transplant and overall response.

Risk factors for arterial versus venous thrombosis in polycythemia vera: a single center experience in 587 patients.

Prognostic implications of abnormalities of chromosome 13 and the presence of multiple cytogenetic high-risk abnormalities in newly diagnosed multiple myeloma.

Prognostic relevance of lymphocytopenia, monocytopenia and lymphocyte-to-monocyte ratio in primary myelodysplastic syndromes: a single center experience in 889 patients.

Prognostic impact of bone marrow fibrosis in polycythemia vera: validation of the IWG-MRT study and additional observations.

Interphase fluorescence in situ hybridization in untreated AL amyloidosis has an independent prognostic impact by abnormality type and treatment category.

Additive value of polygenic risk and family history for coronary heart disease risk stratification in two diverse US cohorts.

Landscape of parental postzygotic mutations across >11,000 rare disease trios.

Likelihood-based calibration improves the clinical utility of JAG1 functional data for variant classification.

Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorder.

Overlapping Xq13.3 duplications define an X-linked hypotrichosis simplex and implicate TAB3 dosage sensitivity.

Bi-allelic variants in CDK20 cause a severe ciliopathy with midline brain and facial anomalies.

Asymmetrical chromosomal utilization during zygotic genome activation.

DeepKaryo-Check: a two-stage automated screening framework for chromosomal numerical and structural abnormalities in clinical karyotype analysis.

Multiparametric analysis of sperm chromatin and ROS reveals the existence of subpopulations that are linked to embryo development after ICSI.

Repeat offenders: Satellite DNA sequence variation drives heterochromatin instability.

Nuclear Dynamics and Its Timing Regulation Revealed by Live-Cell Imaging.

Oocyte Kinetochores at the Nexus of Meiotic Drive and Segregation Fidelity.

Related Experiment Videos

A postulated mechanism for deletions with inversions

Related Concept Videos

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