Chromosome studies in man: past achievements and recent advances

Cryptic deletions and inversions of chromosome 21 in a phenotypically normal infant with transient abnormal myelopoiesis: a molecular cytogenetic study.

British journal of haematology·1998

Deletions of chromosome 21 restricted to the leukemic cells of children with Down syndrome and leukemia.

Leukemia·1997

Haematological abnormalities in Shwachman-Diamond syndrome.

British journal of haematology·1996

Kostmann's disease, recombinant HuG-CSF, monosomy 7 and MDS/AML.

British journal of haematology·1995

Pediatric myelodysplasia: a study of 68 children and a new prognostic scoring system.

Blood·1995

A case of acute megakaryoblastic leukaemia with t(X;6)(p11.21;q23) having an X chromosome breakpoint within a 450-Kb region which is also disrupted in two classes of solid tumours.

Leukemia·1995

ALK overexpression without rearrangement widely exists in EWSR1/FUS-rearranged soft tissue tumours.

Journal of clinical pathology·2026

Adapt or Become Irrelevant: the Pathologist as the new Diagnostic Architect.

Journal of clinical pathology·2026

Targeted transcriptome profiling of oral cavity squamous cell carcinoma and histologic grade-associated gene expression patterns.

Journal of clinical pathology·2026

Retrospective analysis of Claudin 18.2 expression in 64 patients with advanced gastrointestinal peritoneal disease: a potential therapeutic target for high-grade appendiceal mucinous carcinoma.

Journal of clinical pathology·2026

Serum versus lithium-heparin plasma for lipid testing: matrix-related bias and calculated LDL-C classification.

Journal of clinical pathology·2026

Beyond root cause analysis: a practical systems engineering approach to incident investigation in histopathology.

Journal of clinical pathology·2026

Chromosome movements in meiotic prophase: regulatory mechanisms and biological roles.

Frontiers in cell and developmental biology·2026

Nuclear diversity in Charophyceae revealed by fluorescence staining and its implications for genome size estimation.

Planta·2026

SANS ankyrin repeats mediate non-classical nuclear import and dictate distinct pathogenic mechanisms.

The FEBS journal·2026

Bone marrow-inspired DLL1-presenting microparticles enhance asymmetric division and maintenance of mouse hematopoietic stem and progenitor cells.

Stem cell reports·2026

Partial trisomy of 1q42.1 and 8q24.3 deletion: a family history.

Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo·2026

A Novel Hemizygous CDX4 Missense Variant Identified in a Taiwanese Man with Severe Teratozoospermia.

Medicina (Kaunas, Lithuania)·2026

Related Experiment Videos

Chromosome studies in man: past achievements and recent advances

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Cryptic deletions and inversions of chromosome 21 in a phenotypically normal infant with transient abnormal myelopoiesis: a molecular cytogenetic study.

Deletions of chromosome 21 restricted to the leukemic cells of children with Down syndrome and leukemia.

Haematological abnormalities in Shwachman-Diamond syndrome.

Kostmann's disease, recombinant HuG-CSF, monosomy 7 and MDS/AML.

Pediatric myelodysplasia: a study of 68 children and a new prognostic scoring system.

A case of acute megakaryoblastic leukaemia with t(X;6)(p11.21;q23) having an X chromosome breakpoint within a 450-Kb region which is also disrupted in two classes of solid tumours.

ALK overexpression without rearrangement widely exists in EWSR1/FUS-rearranged soft tissue tumours.

Adapt or Become Irrelevant: the Pathologist as the new Diagnostic Architect.

Targeted transcriptome profiling of oral cavity squamous cell carcinoma and histologic grade-associated gene expression patterns.

Retrospective analysis of Claudin 18.2 expression in 64 patients with advanced gastrointestinal peritoneal disease: a potential therapeutic target for high-grade appendiceal mucinous carcinoma.

Serum versus lithium-heparin plasma for lipid testing: matrix-related bias and calculated LDL-C classification.

Beyond root cause analysis: a practical systems engineering approach to incident investigation in histopathology.

Chromosome movements in meiotic prophase: regulatory mechanisms and biological roles.

Nuclear diversity in Charophyceae revealed by fluorescence staining and its implications for genome size estimation.

SANS ankyrin repeats mediate non-classical nuclear import and dictate distinct pathogenic mechanisms.

Bone marrow-inspired DLL1-presenting microparticles enhance asymmetric division and maintenance of mouse hematopoietic stem and progenitor cells.

Partial trisomy of 1q42.1 and 8q24.3 deletion: a family history.

A Novel Hemizygous CDX4 Missense Variant Identified in a Taiwanese Man with Severe Teratozoospermia.

Related Experiment Videos

Chromosome studies in man: past achievements and recent advances

Related Concept Videos

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