[Relationship between chromosome Y and the nucleolus in the peripheral blood lymphocytes]

Congenital heart defects in the recurrent 2q13 deletion syndrome.

European journal of medical genetics·2021

Atrioventricular canal defect and genetic syndromes: The unifying role of sonic hedgehog.

Clinical genetics·2018

Intrafamiliar clinical variability of circumferential skin creases Kunze type caused by a novel heterozygous mutation of N-terminal TUBB gene.

Clinical genetics·2018

Expanding the clinical and molecular spectrum of PRMT7 mutations: 3 additional patients and review.

Clinical genetics·2017

Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome.

Clinical genetics·2017

Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 Mutations.

Molecular syndromology·2013

Cusatuzumab combined with venetoclax with or without azacitidine in unfit patients with newly diagnosed acute myeloid leukemia: phase Ib ELEVATE study.

Haematologica·2026

Surveying survival: benchmarking acute myeloid leukemia outcomes without transplant.

Haematologica·2026

Measurable residual KMT2A partial tandem duplication before allogeneic stem cell transplantation in acute myeloid leukemia.

Haematologica·2026

Normal platelet function in a patient with ARHGEF1 deficiency.

Haematologica·2026

Bone marrow biopsy characteristics at nadir after intensive induction therapy do not predict outcomes in adult acute myeloid leukemia patients: an analysis of ECOG-ACRIN clinical trials.

Haematologica·2026

Efficacy and safety of bridging therapy prior to CAR T-cell therapy in relapsed or refractory multiple myeloma.

Haematologica·2026

Replication stress links Geminin depletion to centrosome amplification.

bioRxiv : the preprint server for biology·2026

Comparative Kd analysis of the interaction between aggregation-prone Nup153 3-2 and KapN.

Journal of magnetic resonance (San Diego, Calif. : 1997)·2026

Organelle partitioning in the multi-budding yeast Aureobasidium pullulans.

Molecular biology of the cell·2026

Pronuclear Transfer and Maternal Spindle Transfer in the Mouse.

Methods in molecular biology (Clifton, N.J.)·2026

Molecular architecture and spatial organization of proteasomes in the human sperm nucleus.

Nature structural & molecular biology·2026

Resolving missing human polymorphic inversions and other complex variants from ultra-long read data.

Genome research·2026

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[Relationship between chromosome Y and the nucleolus in the peripheral blood lymphocytes]

Related Concept Videos

Congenital heart defects in the recurrent 2q13 deletion syndrome.

Atrioventricular canal defect and genetic syndromes: The unifying role of sonic hedgehog.

Intrafamiliar clinical variability of circumferential skin creases Kunze type caused by a novel heterozygous mutation of N-terminal TUBB gene.

Expanding the clinical and molecular spectrum of PRMT7 mutations: 3 additional patients and review.

Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome.

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Cusatuzumab combined with venetoclax with or without azacitidine in unfit patients with newly diagnosed acute myeloid leukemia: phase Ib ELEVATE study.

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Measurable residual KMT2A partial tandem duplication before allogeneic stem cell transplantation in acute myeloid leukemia.

Normal platelet function in a patient with ARHGEF1 deficiency.

Bone marrow biopsy characteristics at nadir after intensive induction therapy do not predict outcomes in adult acute myeloid leukemia patients: an analysis of ECOG-ACRIN clinical trials.

Efficacy and safety of bridging therapy prior to CAR T-cell therapy in relapsed or refractory multiple myeloma.

Replication stress links Geminin depletion to centrosome amplification.

Comparative Kd analysis of the interaction between aggregation-prone Nup153 3-2 and KapN.

Organelle partitioning in the multi-budding yeast Aureobasidium pullulans.

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[Relationship between chromosome Y and the nucleolus in the peripheral blood lymphocytes]

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