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Trisomy 19

A chromosomal abnormality consisting of the presence of a third copy of chromosome 19 in somatic cells.
National Institutes of Health

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Chromosomes, Human, Pair 19

Papers overview

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2012
2012
Coexistence of trisomies of chromosomes 12 and 19 in chronic lymphocytic leukemia occurs exclusively in the rare IgG-positive variant
Citation for published version (APA): Ibbotson, R., Athanasiadou, A., Sutton, L-A., Davis, Z., Gardiner, A., Baliakas, P… 
2007
2007
Trisomy 19 is associated with trisomy 12 and mutated IGHV genes in B‐chronic lymphocytic leukaemia
The occurrence of trisomy 19 was investigated in 705 cases of B‐chronic lymphocytic leukaemia (CLL) by metaphase cytogenetic and… 
2007
2007
Trisomy 19 ependymoma, a newly recognized genetico-histological association, including clear cell ependymoma
Ependymal tumors constitute a clinicopathologically heterogeneous group of brain tumors. They vary in regard to their age at… 
2002
2002
Chromosome 19 abnormalities are commonly seen in AML, M7.
A recent paper by Dastugue et al[1][1] reported the cytogenetic profile of 53 patients with acute megakaryoblastic leukemia (FAB… 
2002
2002
Bcr/Abl, leukemogenesis, and genomic instability: a complex partnership.
Review
1994
Review
1994
Developmental characteristics of trisomy 19 mice.
Trisomy 19 (Ts19), the only murine trisomy compatible with survival beyond birth, allows systematic studies on the effect of an… 
1984
1984
Morphologic development of the fetal trisomy 19 mouse.
Trisomy 19 mice show a characteristic pattern of delayed morphologic development when compared with normal littermates during the… 
1982
1982
Growth characteristics of the murine trisomy 19 thymus.
Development of the trisomy 19 mouse thymus was studied by (1) evaluation of cell and nuclear counts and volume distributions and… 
1981
1981
Mosaic trisomy 19 syndrome.
A stillborn male infant with mosaic trisomy 19 (46,XY/47,XY,+19) is reported. The prenatal ultrasound revealed polyhydramnios… 
1975
1975
Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat.
The case is presented of an infant who was diagnosed clinically as trisomy 18 with pseudohermaphroditism. Cytogenetic studies… 
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