Skip to search formSkip to main contentSkip to account menu

Trisomy 19

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

Related topics

Related topics

1 relation
Chromosomes, Human, Pair 19

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2002
2002
Bcr/Abl, leukemogenesis, and genomic instability: a complex partnership.
2000
2000
Prenatal diagnosis of a partial trisomy 19q
Phenotypic anomalies due to a genetic imbalance of chromosome 19 have been reported in very rare postnatal cases. Here a case of… 
1989
1989
Chromosomal characteristics of Ph-positive chronic myelogenous leukemia in transformation. A study of 23 Chinese patients in Taiwan.
1986
1986
Correlations between immunological phenotype and karyotype in malignant lymphoma.
We have correlated immunological characteristics and karyotypic abnormalities from lymphomas in 118 patients. T-lymphomas… 
1986
1986
Two-dimensional gel analysis of proteins from mouse fetuses with trisomy 19 after DEAE-Sepharose chromatography.
Isoelectrofocusing two-dimensional polyacrylamide gel electrophoresis (IEF-2D-PAGE) offers the opportunity to detect typical… 
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… 
1979
1979
New Translocations in Chronic Granulocytic Leukaemia: t(X;22) (p22;q11) and t(15;22) (q26;q11)
Summary. Two cases of Ph1‐positive chronic granulocytic leukaemia with hitherto undescribed translocations are presented. In case… 
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… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)