Endomitosis in human trophoblast?

Aneuploidy in carcinomas may be initiated by the acquisition of a single trisomy.

Cytogenetic and genome research·2003

Frequency of hyperdiploid chromosome complements in endometrioid tumors of the endometrium whereas similar tumors in the ovary tend to show hypodiploidy: a significant difference that may not be distinguishable by flow cytometry of DNA content.

Cytogenetic and genome research·2002

Microsatellite instability.

Cytogenetics and cell genetics·2001

Significance of chromosome 5 and 17 changes in the development of carcinoma of the cervix uteri.

Cytogenetics and cell genetics·2001

Chromosomal doubling: the significance of polyploidization in the development of human tumors: possibly relevant findings on a lymphoma.

Cancer genetics and cytogenetics·2000

A 3-cM commonly deleted region in 6q21 in leukemias and lymphomas delineated by fluorescence in situ hybridization.

Genes, chromosomes & cancer·1999

The NeuroWES project: lessons learned from comprehensive phenotyping and genetic analysis of neurodevelopmental disorders over a decade.

Human genetics·2026

Implementation of exome sequencing for rare undiagnosed diseases in LMICs: the G2MC rare diseases exome sequencing pilot project.

Human genetics·2026

A novel pathogenic synonymous DHCR7 variant unveiled by aberrant splicing in Smith-Lemli-Opitz syndrome.

Human genetics·2026

Blending borders: reconstructing the genetic history of the Sindhi population.

Human genetics·2026

Within-sibling attenuation of polygenic risk score accuracy: investigating the effects of principal component analysis, LD score regression, and mixed model association in the UK Biobank.

Human genetics·2026

Long-read genome sequencing resolves a de novo complex 18q12.1q21.2 triplication causing partial tetrasomy and reveals its underlying mechanism.

Human genetics·2026

Prenatal Fetal Growth Restriction and Cardiomyopathy Associated With an Unbalanced der(15)t(7;15): A Case Report.

Clinical case reports·2026

Primary Abdominal Ectopic Pregnancy Involving the Spleen: A Case Study.

Case reports in obstetrics and gynecology·2026

Frequency and Subtypes of <i>Blastocystis</i> in Patients with Diarrhea in Van, Türkiye 2022-2023.

Iranian journal of parasitology·2026

The Frequency of Severe Hemolytic Disease of the Fetus and Newborn Caused by Red Blood Cell Alloantibodies Undetected at the Antibodies Screening in the First Trimester: A Prospective Study.

Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie·2026

Endocardial Fibroelastosis as an Early and Isolated Ultrasound Marker of Anti-Ro/SSA(B) Antibodies in the Fetus.

Journal of clinical ultrasound : JCU·2026

Comparison between oral dydrogesterone versus no drugs in clinical outcome within the natural cycle-frozen-thawed embryo transfer cycle: a retrospective analysis.

BMC pregnancy and childbirth·2026

Related Experiment Videos

Endomitosis in human trophoblast?

Related Concept Videos

Aneuploidy in carcinomas may be initiated by the acquisition of a single trisomy.

Frequency of hyperdiploid chromosome complements in endometrioid tumors of the endometrium whereas similar tumors in the ovary tend to show hypodiploidy: a significant difference that may not be distinguishable by flow cytometry of DNA content.

Microsatellite instability.

Significance of chromosome 5 and 17 changes in the development of carcinoma of the cervix uteri.

Chromosomal doubling: the significance of polyploidization in the development of human tumors: possibly relevant findings on a lymphoma.

A 3-cM commonly deleted region in 6q21 in leukemias and lymphomas delineated by fluorescence in situ hybridization.

The NeuroWES project: lessons learned from comprehensive phenotyping and genetic analysis of neurodevelopmental disorders over a decade.

Implementation of exome sequencing for rare undiagnosed diseases in LMICs: the G2MC rare diseases exome sequencing pilot project.

A novel pathogenic synonymous DHCR7 variant unveiled by aberrant splicing in Smith-Lemli-Opitz syndrome.

Blending borders: reconstructing the genetic history of the Sindhi population.

Within-sibling attenuation of polygenic risk score accuracy: investigating the effects of principal component analysis, LD score regression, and mixed model association in the UK Biobank.

Long-read genome sequencing resolves a de novo complex 18q12.1q21.2 triplication causing partial tetrasomy and reveals its underlying mechanism.

Prenatal Fetal Growth Restriction and Cardiomyopathy Associated With an Unbalanced der(15)t(7;15): A Case Report.

Primary Abdominal Ectopic Pregnancy Involving the Spleen: A Case Study.

Frequency and Subtypes of <i>Blastocystis</i> in Patients with Diarrhea in Van, Türkiye 2022-2023.

The Frequency of Severe Hemolytic Disease of the Fetus and Newborn Caused by Red Blood Cell Alloantibodies Undetected at the Antibodies Screening in the First Trimester: A Prospective Study.

Endocardial Fibroelastosis as an Early and Isolated Ultrasound Marker of Anti-Ro/SSA(B) Antibodies in the Fetus.

Comparison between oral dydrogesterone versus no drugs in clinical outcome within the natural cycle-frozen-thawed embryo transfer cycle: a retrospective analysis.

Related Experiment Videos

Endomitosis in human trophoblast?

Related Concept Videos

Related Articles