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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

Papers overview

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Highly Cited
2013
Highly Cited
2013
In this study, we evaluated the impact of secondary genetic lesions in acute myeloid leukemia (AML) with inv(16)(p13.1q22) or t… Expand
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2003
2003
Trisomy rescue is one of various proposed mechanisms in formation of supernumerary small marker chromosomes (SMC) and uniparental… Expand
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2001
2001
Chondrosarcomas are malignant cartilaginous tumors. Most are located in the medullar cavity (central chondrosarcoma), and a… Expand
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1995
1995
We describe a term infant with facioauriculo-vertebral "dysplasia" (Goldenhar sequence), hypertelorism, and mosaic trisomy 22… Expand
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Review
1993
Review
1993
We report on an infant girl born with complete trisomy 22 and left hemifacial microsomia, ear anomaly, and limbal and epibulbar… Expand
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Highly Cited
1989
Highly Cited
1989
Chorionic villus sampling is a method of prenatal diagnosis in the first trimester of pregnancy in which tissue for genetic study… Expand
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1981
1981
SummaryA severely growth-retarded female newborn is described, who died a few hours after birth. About half of the clones and… Expand
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1973
1973
SummaryUsing quinacrine fluorescence and Giemsa banding techniques we have identified an extra chromosome 22 in three non… Expand
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1972
1972
SummaryA family is presented in which a phenotypically normal mother and her healthy daughter both had abnormal children with a… Expand
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1971
1971
The constellation of a characteristic facies, mental retardation, growth retardation,microcephaly, micrognathia, preauricular… Expand
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