Triple trisomy in a spontaneous abortion

Cytogenetic and molecular studies of Down syndrome individuals with leukemia.

American journal of human genetics·1995

Trisomy 2 and 20 in two hepatoblastomas.

Genes, chromosomes & cancer·1991

A familial MCA/MR syndrome due to translocation t(10;16) (q26;p13.1): report of six cases.

American journal of medical genetics·1991

Continuous human glioma-derived cell lines UC-11MG and UC-302MG. Morphologic, immunocytochemical and chromosomal characterization.

Journal of neuro-oncology·1986

Biologic characteristics of four Ewing's sarcomas.

Cancer genetics and cytogenetics·1985

Chromosome features of two retinoblastomas.

Cancer genetics and cytogenetics·1984

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.

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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

Mystery Client Methodologies to Evaluate Abortion Care and Access: A Scoping Review.

Healthcare (Basel, Switzerland)·2026

A Case of Thrombocytopenia, Anasarca, Fever, Reticulin Fibrosis/Renal Dysfunction, and Organomegaly (TAFRO) Syndrome Refractory to Treatment With Combination Therapy of Corticosteroid, Tocilizumab, and Rituximab: A Case Report.

Cureus·2026

Insertion of Subdermal Hormonal Implant May Trigger Complex Regional Pain Syndrome: A Case Report.

The Journal of adolescent health : official publication of the Society for Adolescent Medicine·2026

Diagnosis of chlamydial and gonococcal conjunctivitis: performance evaluation of a nucleic acid amplification test.

Microbiology spectrum·2026

Limited Availability of Short Tandem Repeat Genotype Testing in the United States for Diagnosis of Partial Hydatidiform Mole: A Dilemma for Practicing Precision Medicine.

The American journal of surgical pathology·2026

Intrauterine Pregnancy With a Correctly Positioned Levonorgestrel-Releasing Intrauterine System: A Case Report.

Cureus·2026

Related Experiment Videos

Triple trisomy in a spontaneous abortion

Related Concept Videos

Cytogenetic and molecular studies of Down syndrome individuals with leukemia.

Trisomy 2 and 20 in two hepatoblastomas.

A familial MCA/MR syndrome due to translocation t(10;16) (q26;p13.1): report of six cases.

Continuous human glioma-derived cell lines UC-11MG and UC-302MG. Morphologic, immunocytochemical and chromosomal characterization.

Biologic characteristics of four Ewing's sarcomas.

Chromosome features of two retinoblastomas.

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.

Mystery Client Methodologies to Evaluate Abortion Care and Access: A Scoping Review.

A Case of Thrombocytopenia, Anasarca, Fever, Reticulin Fibrosis/Renal Dysfunction, and Organomegaly (TAFRO) Syndrome Refractory to Treatment With Combination Therapy of Corticosteroid, Tocilizumab, and Rituximab: A Case Report.

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Limited Availability of Short Tandem Repeat Genotype Testing in the United States for Diagnosis of Partial Hydatidiform Mole: A Dilemma for Practicing Precision Medicine.

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Triple trisomy in a spontaneous abortion

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