Trisomy for the short arm of chromosome No. 10

Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone disease.

American journal of medical genetics·2001

Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p.

Genetic counseling (Geneva, Switzerland)·2000

Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas. Possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1q.

Cancer genetics and cytogenetics·1999

Sperm analysis in a subfertile male with a Y;16 translocation, using four-color FISH.

Cytogenetics and cell genetics·1999

Subfertile men with constitutive chromosome abnormalities do not necessarily refrain from intracytoplasmic sperm injection treatment: a follow-up study on 75 Dutch patients.

Human reproduction (Oxford, England)·1999

One normal child and a chromosomally balanced/normal twin after intracytoplasmic sperm injection in a male with a de-novo t(Y;16) translocation.

Human reproduction (Oxford, England)·1998

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

Clinical genetics·2026

A Novel De Novo STAG1 Variant at the RAD21 Binding Interface Is Associated With Hypoglycemia, Recurrent Fever, Immunodeficiency and Features of Classical Cohesinopathies.

Clinical genetics·2026

Pathogenicity of NUSAP1 Variants Is Defined by NMD-Escape: Evidence From Two Novel Cases and Systematic Population-Based Variant Analysis.

Clinical genetics·2026

Biallelic ABCA13 Loss-of-Function Variants in a Child With Neurodevelopmental Delay: A Case Report.

Clinical genetics·2026

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Clinical genetics·2026

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Clinical genetics·2026

Demographic shifts in referral to and completion of lung cancer screening after the 2021 United States Preventive Services Task Force update.

Journal of thoracic disease·2026

Effectiveness of Virtual Reality in Supporting Informal Caregivers: A Protocol for a Systematic Review and Meta-Analysis.

Campbell systematic reviews·2026

Personalizing health call center services: results from an online survey on user experiences in Kuwait.

F1000Research·2026

Associations between perceived organizational support, workplace violence, and employee outcomes: a cross-sectional study.

Frontiers in psychology·2026

Patterns of Cohort Participation Among People with Systemic Sclerosis in an Open Cohort: a Scleroderma Patient-centered Intervention Network Cohort Study.

American journal of epidemiology·2026

A Pilot Evaluation of a Web-Based Intervention Aiming to Improve Employer Confidence in Hiring Autistic People.

Autism : the international journal of research and practice·2026

Related Experiment Videos

Trisomy for the short arm of chromosome No. 10

Related Concept Videos

Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone disease.

Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p.

Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas. Possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1q.

Sperm analysis in a subfertile male with a Y;16 translocation, using four-color FISH.

Subfertile men with constitutive chromosome abnormalities do not necessarily refrain from intracytoplasmic sperm injection treatment: a follow-up study on 75 Dutch patients.

One normal child and a chromosomally balanced/normal twin after intracytoplasmic sperm injection in a male with a de-novo t(Y;16) translocation.

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

A Novel De Novo STAG1 Variant at the RAD21 Binding Interface Is Associated With Hypoglycemia, Recurrent Fever, Immunodeficiency and Features of Classical Cohesinopathies.

Pathogenicity of NUSAP1 Variants Is Defined by NMD-Escape: Evidence From Two Novel Cases and Systematic Population-Based Variant Analysis.

Biallelic ABCA13 Loss-of-Function Variants in a Child With Neurodevelopmental Delay: A Case Report.

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Demographic shifts in referral to and completion of lung cancer screening after the 2021 United States Preventive Services Task Force update.

Effectiveness of Virtual Reality in Supporting Informal Caregivers: A Protocol for a Systematic Review and Meta-Analysis.

Personalizing health call center services: results from an online survey on user experiences in Kuwait.

Associations between perceived organizational support, workplace violence, and employee outcomes: a cross-sectional study.

Patterns of Cohort Participation Among People with Systemic Sclerosis in an Open Cohort: a Scleroderma Patient-centered Intervention Network Cohort Study.

A Pilot Evaluation of a Web-Based Intervention Aiming to Improve Employer Confidence in Hiring Autistic People.

Related Experiment Videos

Trisomy for the short arm of chromosome No. 10

Related Concept Videos

Related Articles