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Chromosome 9, trisomy

Known as: Chromosome 9 trisomy, Duplication 9, Trisomy 9 
A chromosomal abnormality consisting of the presence of a third copy of chromosome 9 in somatic cells.
National Institutes of Health

Papers overview

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2005
2005
phenotype. Trisomy 16q is usually the result of a maternal translocation (Masuno et al., 2000). Most reported cases with 22q13… 
1993
1993
  • A. Schinzel
  • 1993
  • Corpus ID: 11156720
1989
1989
The proband, an 18 month old child, was delivered by caesarian section after an uneventful 38 week gestation, birth weight 2400 g… 
Review
1985
Review
1985
A case of trisomy 9 showing a complex cardiac malformation is presented with a review of other published cases. A distinct… 
1982
1982
A clinical and pathologic study of a neonate with mosaic trisomy 9 revealed findings similar to those in other cases with this… 
1982
1982
Amniocentesis was performed on a 39-year-old gravida 4 woman because of maternal age. Ultrasonography demonstrated a twin… 
1977
1977
Two sibs are reported with partial trisomy 9, the consequence of a maternal reciprocal translocation. 
1974
1974
SummaryAutoradiographic investigation of the cell cycle of 12 diploid and 12 abnormal human fibroblast strains was carried out… 
1973
1973
A phenotypically normal woman has an apparently balanced reciprocal translocation between chromosomes No. 9 and No. 18…