Frequency of chromosomal abnormalities in miscarriages and perinatal deaths

Sex ratio and absence of uniparental disomy in spontaneous abortions with a normal karyotype.

Clinical genetics·1998

Solid tissue culture for cytogenetic analysis: a collaborative survey for the Association of Clinical Cytogeneticists.

Journal of clinical pathology·1996

Rapid prenatal diagnosis of Patau's syndrome in a fetus with an abdominal wall defect by 72 hour culture of cells from amniotic fluid.

Prenatal diagnosis·1993

Premature chromosome condensation in childhood acute lymphoblastic leukaemia: correlation of proliferative potential index in blood and marrow.

Genes, chromosomes & cancer·1989

Are double translocations double trouble?

Journal of medical genetics·1988

Annual statistical review.

Archives of disease in childhood·1987

Childhood-onset neurodegeneration and brain atrophy: defining UBTF-related developmental regression and progressive ataxia.

Journal of medical genetics·2026

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Journal of medical genetics·2026

Evolving roles within the genomic medicine workforce: a revised framework for UK practice-position on behalf of the Association of Genetic Nurses and Counsellors and the Clinical Genetics Society.

Journal of medical genetics·2026

Actionable genotypes beyond the coding sequence and their association with lifespan in the UK Biobank.

Journal of medical genetics·2026

Pan-ethnic preconception screening: evidence from a large-scale programme in a genetically diverse population.

Journal of medical genetics·2026

CACNA1C variants associated with focal epilepsy and their correlations with arrhythmias and developmental disorders.

Journal of medical genetics·2026

Cardiac volumes, function, and arterial stiffness five years after severe preeclampsia: A comparison with sedentary and active controls.

Clinical physiology and functional imaging·2026

A Case Report of a Spontaneous Angular Pregnancy: A Diagnostic Challenge.

Cureus·2026

A novel circular RNA hsa_circ_0079474 facilitates intrauterine adhesion by targeting miR-630/YAP1 axis to stimulate epithelial-mesenchymal transition.

Molecular human reproduction·2026

Immunohistochemical and Ultrastructural Evaluation of Human Fetal Testicular Development Across Different Gestational Ages.

Cureus·2026

High-risk pulmonary embolism in the first trimester of pregnancy: Successful thrombolysis with tenecteplase.

Radiology case reports·2026

Rare variant of Zinner syndrome with ectopic seminal vesicle and prostatic hypoplasia: A case report.

Radiology case reports·2026

Related Experiment Videos

Frequency of chromosomal abnormalities in miscarriages and perinatal deaths

Related Concept Videos

Sex ratio and absence of uniparental disomy in spontaneous abortions with a normal karyotype.

Solid tissue culture for cytogenetic analysis: a collaborative survey for the Association of Clinical Cytogeneticists.

Rapid prenatal diagnosis of Patau's syndrome in a fetus with an abdominal wall defect by 72 hour culture of cells from amniotic fluid.

Premature chromosome condensation in childhood acute lymphoblastic leukaemia: correlation of proliferative potential index in blood and marrow.

Are double translocations double trouble?

Annual statistical review.

Childhood-onset neurodegeneration and brain atrophy: defining UBTF-related developmental regression and progressive ataxia.

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Evolving roles within the genomic medicine workforce: a revised framework for UK practice-position on behalf of the Association of Genetic Nurses and Counsellors and the Clinical Genetics Society.

Actionable genotypes beyond the coding sequence and their association with lifespan in the UK Biobank.

Pan-ethnic preconception screening: evidence from a large-scale programme in a genetically diverse population.

CACNA1C variants associated with focal epilepsy and their correlations with arrhythmias and developmental disorders.

Cardiac volumes, function, and arterial stiffness five years after severe preeclampsia: A comparison with sedentary and active controls.

A Case Report of a Spontaneous Angular Pregnancy: A Diagnostic Challenge.

A novel circular RNA hsa_circ_0079474 facilitates intrauterine adhesion by targeting miR-630/YAP1 axis to stimulate epithelial-mesenchymal transition.

Immunohistochemical and Ultrastructural Evaluation of Human Fetal Testicular Development Across Different Gestational Ages.

High-risk pulmonary embolism in the first trimester of pregnancy: Successful thrombolysis with tenecteplase.

Rare variant of Zinner syndrome with ectopic seminal vesicle and prostatic hypoplasia: A case report.

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Frequency of chromosomal abnormalities in miscarriages and perinatal deaths

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