Partial duplication of the long arm of chromosome 4

Posterior scalp defects in Opitz syndrome. Another symptom related to a defect in midline development.

Clinical genetics·1992

The primary sequence and the subunit structure of mouse alpha-2-macroglobulin, deduced from protein sequencing of the isolated subunits and from molecular cloning of the cDNA.

European journal of biochemistry·1992

Developmental changes in heparan sulfate expression: in situ detection with mAbs.

The Journal of cell biology·1992

Leukaemic intermediate lymphocytic lymphomas: analysis of twelve cases diagnosed by morphology.

Leukemia & lymphoma·1992

Trisomy 7 and trisomy 10 characterize subpopulations of tumor-infiltrating lymphocytes in kidney tumors and in the surrounding kidney tissue.

Proceedings of the National Academy of Sciences of the United States of America·1992

Cell surface heparan sulfate proteoglycans from human vascular endothelial cells. Core protein characterization and antithrombin III binding properties.

The Journal of biological chemistry·1992

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Annales de genetique·2004

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Annales de genetique·2004

Large duplication 4q25-q34 with mild clinical effect.

Annales de genetique·2004

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Annales de genetique·2004

Partial trisomy 8q and partial monosomy 18p: a case report.

Annales de genetique·2004

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

Annales de genetique·2004

Excess mortality convergence after paediatric allogeneic transplantation: a caveat for the right to be forgotten. Comment on: "Decreasing excess mortality after allogeneic stem cell transplantation for acute leukemia".

Haematologica·2026

Pediatric orbital solitary fibrous tumor/hemangiopericytoma presenting with isolated eyelid edema: a case report.

Frontiers in pediatrics·2026

Closed reduction technique for complex dorsal metacarpophalangeal dislocation in children.

The Journal of hand surgery, European volume·2026

A Phase 3 Trial of Vosoritide in Children with Hypochondroplasia.

NEJM evidence·2026

When rare diseases do not appear as a single entity.

Advances in laboratory medicine·2026

Proximal Tibial Giant Cell Tumor in a Skeletally Immature Child: A Diagnostic Dilemma and Review of the Literature.

Journal of orthopaedic case reports·2026

Related Experiment Videos

Partial duplication of the long arm of chromosome 4

Related Concept Videos

Posterior scalp defects in Opitz syndrome. Another symptom related to a defect in midline development.

The primary sequence and the subunit structure of mouse alpha-2-macroglobulin, deduced from protein sequencing of the isolated subunits and from molecular cloning of the cDNA.

Developmental changes in heparan sulfate expression: in situ detection with mAbs.

Leukaemic intermediate lymphocytic lymphomas: analysis of twelve cases diagnosed by morphology.

Trisomy 7 and trisomy 10 characterize subpopulations of tumor-infiltrating lymphocytes in kidney tumors and in the surrounding kidney tissue.

Cell surface heparan sulfate proteoglycans from human vascular endothelial cells. Core protein characterization and antithrombin III binding properties.

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Large duplication 4q25-q34 with mild clinical effect.

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Partial trisomy 8q and partial monosomy 18p: a case report.

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

Excess mortality convergence after paediatric allogeneic transplantation: a caveat for the right to be forgotten. Comment on: "Decreasing excess mortality after allogeneic stem cell transplantation for acute leukemia".

Pediatric orbital solitary fibrous tumor/hemangiopericytoma presenting with isolated eyelid edema: a case report.

Closed reduction technique for complex dorsal metacarpophalangeal dislocation in children.

A Phase 3 Trial of Vosoritide in Children with Hypochondroplasia.

When rare diseases do not appear as a single entity.

Proximal Tibial Giant Cell Tumor in a Skeletally Immature Child: A Diagnostic Dilemma and Review of the Literature.

Related Experiment Videos

Partial duplication of the long arm of chromosome 4

Abstract:

Related Concept Videos

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