Aneuploidy of chromosome X, variants 22 and fra(17p12)

Chronic Myelogenous Leukemia Associated with Extranodal B-Cell Lymphoma.

Leukemia & lymphoma·2016

CD8 T cell-mediated rejection of intestinal allografts is resistant to inhibition of the CD40/CD154 costimulatory pathway.

Transplantation·2001

The role of CDP in the negative regulation of CXCL1 gene expression.

The Journal of biological chemistry·2001

Dysplasia as a predictive marker for invasive carcinoma in Barrett esophagus: a follow-up study based on 138 cases from a diagnostic variability study.

Human pathology·2001

Reproducibility of the diagnosis of dysplasia in Barrett esophagus: a reaffirmation.

Human pathology·2001

Effects of educational and psychosocial interventions for adolescents with diabetes mellitus: a systematic review.

Health technology assessment (Winchester, England)·2001

Two Truncating MITF Variants Expand the Phenotypic Spectrum of COMMAD Syndrome.

Clinical genetics·2026

Compound-Heterozygous PLVAP Missense Variants Associated With Attenuated Protein-Losing Enteropathy (DIAR10).

Clinical genetics·2026

A Novel ACAN Missense Variant in the G1 Domain Causes Short Stature, Advanced Bone Age, and Osteochondritis Dissecans: A Case Report and Literature Review.

Clinical genetics·2026

A De Novo ATP1A3 p.Arg995His Variant in a Patient With an Adult-Onset Primary Lateral Sclerosis-Like Syndrome.

Clinical genetics·2026

A Homozygous Frameshift Variant in KHDC4 Is Associated With a Syndromic Inherited Retinal Disease in Humans.

Clinical genetics·2026

Müllerian Duct Aplasia in a Girl With SMARCB1-Related Coffin-Siris Syndrome: A Rare Co-Occurring Anomaly.

Clinical genetics·2026

A practical HPLC-UV method for the simultaneous screening of decabromodiphenyl ethane and its debromination products in environmental matrices.

Analytical methods : advancing methods and applications·2026

Finger-prick whole blood analysis via surface-enhanced Raman spectroscopy using centrifugal silver plasmonic paper substrates.

Analytica chimica acta·2026

Status epilepticus as a novel etiology of Lance-Adams syndrome: a case report.

Epilepsy & behavior reports·2026

Colorimetric analysis of Cu2+ ions using a halochromic indicator solution and an electrospun film prepared using Caesalpinia sappan L.

Analytical methods : advancing methods and applications·2026

Visualized separation of exosomes in urine using carrier ampholyte-free free-flow isoelectric focusing electrophoresis.

Journal of chromatography. A·2026

A dual-electropolymerized poly(Xylenol orange)@poly(Euchrysine) sensing interface for sustainable simultaneous electroanalysis of 5-fluorouracil and empagliflozin: density functional theory mechanistic elucidation.

Mikrochimica acta·2026

Related Experiment Videos

Aneuploidy of chromosome X, variants 22 and fra(17p12)

Related Concept Videos

Chronic Myelogenous Leukemia Associated with Extranodal B-Cell Lymphoma.

CD8 T cell-mediated rejection of intestinal allografts is resistant to inhibition of the CD40/CD154 costimulatory pathway.

The role of CDP in the negative regulation of CXCL1 gene expression.

Dysplasia as a predictive marker for invasive carcinoma in Barrett esophagus: a follow-up study based on 138 cases from a diagnostic variability study.

Reproducibility of the diagnosis of dysplasia in Barrett esophagus: a reaffirmation.

Effects of educational and psychosocial interventions for adolescents with diabetes mellitus: a systematic review.

Two Truncating MITF Variants Expand the Phenotypic Spectrum of COMMAD Syndrome.

Compound-Heterozygous PLVAP Missense Variants Associated With Attenuated Protein-Losing Enteropathy (DIAR10).

A Novel ACAN Missense Variant in the G1 Domain Causes Short Stature, Advanced Bone Age, and Osteochondritis Dissecans: A Case Report and Literature Review.

A De Novo ATP1A3 p.Arg995His Variant in a Patient With an Adult-Onset Primary Lateral Sclerosis-Like Syndrome.

A Homozygous Frameshift Variant in KHDC4 Is Associated With a Syndromic Inherited Retinal Disease in Humans.

Müllerian Duct Aplasia in a Girl With SMARCB1-Related Coffin-Siris Syndrome: A Rare Co-Occurring Anomaly.

A practical HPLC-UV method for the simultaneous screening of decabromodiphenyl ethane and its debromination products in environmental matrices.

Finger-prick whole blood analysis via surface-enhanced Raman spectroscopy using centrifugal silver plasmonic paper substrates.

Status epilepticus as a novel etiology of Lance-Adams syndrome: a case report.

Colorimetric analysis of Cu2+ ions using a halochromic indicator solution and an electrospun film prepared using Caesalpinia sappan L.

Visualized separation of exosomes in urine using carrier ampholyte-free free-flow isoelectric focusing electrophoresis.

A dual-electropolymerized poly(Xylenol orange)@poly(Euchrysine) sensing interface for sustainable simultaneous electroanalysis of 5-fluorouracil and empagliflozin: density functional theory mechanistic elucidation.

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Aneuploidy of chromosome X, variants 22 and fra(17p12)

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