Non-fluorescent Y-chromosome in mixed gonadal dysgenesis with 45,X/46,XY mosaicism

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

[The floating kidney: a rare cause of abdominal pain].

Nederlands tijdschrift voor geneeskunde·2026

Corifollitropin alfa versus daily recombinant FSH for ovarian stimulation in women of advanced maternal age: a cost-minimization analysis in an out-of-pocket setting.

Frontiers in reproductive health·2026

Absence of hymenal trauma does not exclude child sexual abuse: Forensic significance of a study-defined highly elastic/dilated hymenal phenotype.

Journal of forensic and legal medicine·2026

Zinner Syndrome Associated With a Neuroendocrine Tumor of the Prostate Gland and Contralateral Seminal Vesicle: A Case Report.

Cureus·2026

Periadrenal mature cystic teratoma mimicking adrenal myelolipoma: a case report and review of the literature.

Journal of surgical case reports·2026

Multiple High-Risk HPV Infections and Opportunistic HPV Prevalence Among Women Aged 18-25 Years with NILM, ASC-US, or LSIL Cytology: A 2024 Cross-Sectional Study.

Pathogens (Basel, Switzerland)·2026

Related Experiment Videos

Non-fluorescent Y-chromosome in mixed gonadal dysgenesis with 45,X/46,XY mosaicism

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.

[The floating kidney: a rare cause of abdominal pain].

Corifollitropin alfa versus daily recombinant FSH for ovarian stimulation in women of advanced maternal age: a cost-minimization analysis in an out-of-pocket setting.

Absence of hymenal trauma does not exclude child sexual abuse: Forensic significance of a study-defined highly elastic/dilated hymenal phenotype.

Zinner Syndrome Associated With a Neuroendocrine Tumor of the Prostate Gland and Contralateral Seminal Vesicle: A Case Report.

Periadrenal mature cystic teratoma mimicking adrenal myelolipoma: a case report and review of the literature.

Multiple High-Risk HPV Infections and Opportunistic HPV Prevalence Among Women Aged 18-25 Years with NILM, ASC-US, or LSIL Cytology: A 2024 Cross-Sectional Study.

Related Experiment Videos

Non-fluorescent Y-chromosome in mixed gonadal dysgenesis with 45,X/46,XY mosaicism

Related Concept Videos

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