Mosaic Trisomy 9 Latest Advances

Acute Myeloid Leukemia With Philadelphia Chromosome and Complex Karyotype: A Diagnostic Dilemma.

Journal: Cureus

Published: May 28, 2026

Case Report: Rare triple-line chromosome 9 mosaicism (47,XX,+del(9)(q13)/47,XX,+9/46,XX) associated with severe neurodevelopmental impairment and congenital anomalies.

Journal: Frontiers in genetics

Published: December 17, 2025

Fetal Double Partial Trisomy 6 and 9 Due to Maternal 3:1 Meiotic Segregation of a Balanced Translocation.

Journal: Clinical laboratory

Published: December 09, 2025

Partial Trisomy of Chromosome 9 Inherited by Adjacent Segregation 2 of a Balanced Reciprocal Translocation in the Mother: Rare Mechanism in Chromosomal Abnormalities.

Journal: Balkan journal of medical genetics : BJMG

Published: November 07, 2025

Genome sequencing-based CNV analysis in an infant with concurrent partial trisomies 9p and 12p due to maternal translocation: A case report.

Journal: Medicine

Published: September 17, 2025

Trisomy 9 mosaicism: a genetic disorder with complications-a case report.

Journal: Journal of medical case reports

Published: April 14, 2025

Presenting Characteristics and Medical Conditions in 67 Cases With Trisomy 9 Mosaicism.

Journal: Clinical genetics

Published: February 17, 2025

A rare case of uniparental disomy 9 concomitant with low-level mosaicism for trisomy 9.

Journal: Vavilovskii zhurnal genetiki i selektsii

Published: February 14, 2025

Non-Mosaic Trisomy 9: Further Delineation of the Clinical Phenotype.

Journal: American journal of medical genetics. Part A

Published: January 07, 2025

Aphallia in a patient with 9q34 duplication syndrome: a case report.

Journal: BMC urology

Published: December 02, 2024

An infant with trisomy 9 and partial trisomy 12 derived from maternal balanced translocation: A case report and literature review.

Journal: The Journal of international medical research

Published: November 29, 2024

Inherited Unbalanced Reciprocal Translocation with 18p11.32p11.21 Tetrasomy and 9q34.3 Trisomy in a Fetus Revealed by Cell-Free Fetal DNA (cffDNA) Testing: Cytogenetic and Cytogenomic Characterization in Prenatal Diagnosis.

Journal: Genes

Published: September 19, 2024

Mosaic Trisomy 9 Latest Advances

Find the Latest Research About Mosaic Trisomy 9

Acute Myeloid Leukemia With Philadelphia Chromosome and Complex Karyotype: A Diagnostic Dilemma.

Acute Myeloid Leukemia With Philadelphia Chromosome and Complex Karyotype: A Diagnostic Dilemma.

Case Report: Rare triple-line chromosome 9 mosaicism (47,XX,+del(9)(q13)/47,XX,+9/46,XX) associated with severe neurodevelopmental impairment and congenital anomalies.

Case Report: Rare triple-line chromosome 9 mosaicism (47,XX,+del(9)(q13)/47,XX,+9/46,XX) associated with severe neurodevelopmental impairment and congenital anomalies.

Fetal Double Partial Trisomy 6 and 9 Due to Maternal 3:1 Meiotic Segregation of a Balanced Translocation.

Fetal Double Partial Trisomy 6 and 9 Due to Maternal 3:1 Meiotic Segregation of a Balanced Translocation.

Partial Trisomy of Chromosome 9 Inherited by Adjacent Segregation 2 of a Balanced Reciprocal Translocation in the Mother: Rare Mechanism in Chromosomal Abnormalities.

Partial Trisomy of Chromosome 9 Inherited by Adjacent Segregation 2 of a Balanced Reciprocal Translocation in the Mother: Rare Mechanism in Chromosomal Abnormalities.

Genome sequencing-based CNV analysis in an infant with concurrent partial trisomies 9p and 12p due to maternal translocation: A case report.

Genome sequencing-based CNV analysis in an infant with concurrent partial trisomies 9p and 12p due to maternal translocation: A case report.

Trisomy 9 mosaicism: a genetic disorder with complications-a case report.

Trisomy 9 mosaicism: a genetic disorder with complications-a case report.

Presenting Characteristics and Medical Conditions in 67 Cases With Trisomy 9 Mosaicism.

Presenting Characteristics and Medical Conditions in 67 Cases With Trisomy 9 Mosaicism.

A rare case of uniparental disomy 9 concomitant with low-level mosaicism for trisomy 9.

A rare case of uniparental disomy 9 concomitant with low-level mosaicism for trisomy 9.

Non-Mosaic Trisomy 9: Further Delineation of the Clinical Phenotype.

Non-Mosaic Trisomy 9: Further Delineation of the Clinical Phenotype.

Aphallia in a patient with 9q34 duplication syndrome: a case report.

Aphallia in a patient with 9q34 duplication syndrome: a case report.

An infant with trisomy 9 and partial trisomy 12 derived from maternal balanced translocation: A case report and literature review.

An infant with trisomy 9 and partial trisomy 12 derived from maternal balanced translocation: A case report and literature review.

Inherited Unbalanced Reciprocal Translocation with 18p11.32p11.21 Tetrasomy and 9q34.3 Trisomy in a Fetus Revealed by Cell-Free Fetal DNA (cffDNA) Testing: Cytogenetic and Cytogenomic Characterization in Prenatal Diagnosis.

Inherited Unbalanced Reciprocal Translocation with 18p11.32p11.21 Tetrasomy and 9q34.3 Trisomy in a Fetus Revealed by Cell-Free Fetal DNA (cffDNA) Testing: Cytogenetic and Cytogenomic Characterization in Prenatal Diagnosis.