Familial paracentric inversion of the short arm of chromosome 3

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

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

Leukemia & lymphoma·1992

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

The Journal of cell biology·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

Cellular level investigation of skin permeation using stimulated Raman scattering microscopy and in-silico modelling.

International journal of pharmaceutics·2026

Application of cellulose sponge modified by polypyrrole for thin film microextraction of polycyclic aromatic hydrocarbons.

Analytical sciences : the international journal of the Japan Society for Analytical Chemistry·2026

Musculoskeletal Histopathology of Klippel-Trénaunay Syndrome: A Clinicopathologic Study of 21 Cases With Long-Term Orthopedic Follow-Up.

The American journal of surgical pathology·2026

[CHYLURIA TREATED BY RETROPERITONEOSCOPIC LYMPHATIC DISCONNECTION: REPORT OF A CASE].

Nihon Hinyokika Gakkai zasshi. The japanese journal of urology·2026

Imaging of Congenital Anomalies of the Spinal Cord: Part 1.

Neuroimaging clinics of North America·2026

An experimental study on hand injury in beer bottle assault: A perpetrator perspective.

Forensic science international·2026

Related Experiment Videos

Familial paracentric inversion of the short arm of chromosome 3

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.

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

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

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.

Cellular level investigation of skin permeation using stimulated Raman scattering microscopy and in-silico modelling.

Application of cellulose sponge modified by polypyrrole for thin film microextraction of polycyclic aromatic hydrocarbons.

Musculoskeletal Histopathology of Klippel-Trénaunay Syndrome: A Clinicopathologic Study of 21 Cases With Long-Term Orthopedic Follow-Up.

[CHYLURIA TREATED BY RETROPERITONEOSCOPIC LYMPHATIC DISCONNECTION: REPORT OF A CASE].

Imaging of Congenital Anomalies of the Spinal Cord: Part 1.

An experimental study on hand injury in beer bottle assault: A perpetrator perspective.

Related Experiment Videos

Familial paracentric inversion of the short arm of chromosome 3

Abstract:

Related Concept Videos

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