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Trisomy 22

Known as: Chromosome 22, trisomy, Duplication 22 
A chromosomal abnormality consisting of the presence of a third copy of chromosome 22 in somatic cells.
National Institutes of Health

Related topics

Related topics

3 relations

Broader (2)

Chromosomes, Human, Pair 22Trisomy
Down Syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2003
2003
Supernumerary small marker chromosome (SMC) and uniparental disomy 22 in a child with confined placental mosaicism of trisomy 22: Trisomy rescue due to marker chromosome formation
Trisomy rescue is one of various proposed mechanisms in formation of supernumerary small marker chromosomes (SMC) and uniparental… 
2001
2001
Chromosome 9 alterations and trisomy 22 in central chondrosarcoma: a cytogenetic and DNA flow cytometric analysis of chondrosarcoma subtypes.
Chondrosarcomas are malignant cartilaginous tumors. Most are located in the medullar cavity (central chondrosarcoma), and a… 
1996
1996
Correlation between karyotype and ultrasound findings in patients with failed early pregnancy
The aim of this retrospective study was to identify any consistent patterns between ultrasound findings in failed pregnancies and… 
Highly Cited
1981
Highly Cited
1981
Incomplete trisomy 22
SummaryTwo brothers with duplication of the distal segment of 22q inherited from a t(6;22)(q27;13) translocation carrier mother… 
Highly Cited
1981
Highly Cited
1981
Incomplete trisomy 22
SummaryA severely growth-retarded female newborn is described, who died a few hours after birth. About half of the clones and… 
1977
1977
Partial trisomy 22: A recognizable syndrome
A patient identified as being a partial trisomy 22 mosaic is presented. The presence of a translocation t(4;22) (pter;q12) is… 
1975
1975
Trisomy 22.
The existence of a trisomy 22 has been definitely established by newer methods of karyotype analysis which permit distinction… 
Review
1975
Review
1975
Trisomy 22. Two new cases and delineation of the phenotype.
Two unrelated children, not affected with Down's syndrome, with strikingly similar phenotypes and an extra G-like chromosome are… 
1974
1974
Prenatal mortality of trisomy 21 (Down's syndrome).
1968
1968
Familial occurrence of trisomy 22.
and is a few 
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