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Trisomy 5
A chromosomal abnormality consisting of the presence of a third copy of chromosome 5 in somatic cells.
National Institutes of Health
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Related topics
Related topics
12 relations
Angioimmunoblastic Lymphadenopathy
Childhood Ganglioglioma
Chromosomes, Human, Pair 5
Cutaneous Angioimmunoblastic T-Cell Lymphoma
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
VACTERL phenotype with mosaic trisomy 5 and uniparental disomy 5
Samuel Hwang
,
M. K. Rudd
,
L. Finch
,
S. Peterson
,
R. Kapur
American Journal of Medical Genetics. Part A
2018
Corpus ID: 46709636
1Department of Pathology, Oregon Health & Science University, Portland, Oregon 2Center for Molecular Biology and Pathology…
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2017
2017
A prenatal diagnosis of mosaic trisomy 5 reveals a postnatal complete uniparental disomy of chromosome 5 with multiple congenital anomalies
Andrew M Reittinger
,
B. Helm
,
D. Boles
,
I. Gadi
,
S. S. Schrier Vergano
American Journal of Medical Genetics. Part A
2017
Corpus ID: 36170511
Mosaic trisomy 5 is a very rare condition in liveborns, with few cases reported in the last four decades. There are some reports…
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2017
2017
[Characteristics and Prognostic Significance of Cytogenetic Abnormalities in Diffuse Large B-Cell Lymphoma Patients with Bone Marrow Involvement].
W. Liu
,
R. Lyu
,
+6 authors
S. Yi
Zhongguo shi yan xue ye xue za zhi
2017
Corpus ID: 30319915
OBJECTIVE To investigate the cytogenetic abnormalitis in patients with diffuse large B-cell lymphoma(DLBCL) patients with bone…
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2011
2011
Full trisomy 5 in a sample of spontaneous abortion and arias stella reaction
V. Čulić
,
B. Lozić
,
I. Kuzmić-Prusac
,
G. Mijaljica
,
J. Pavelić
Medical Science Monitor
2011
Corpus ID: 8397946
Summary Background Historically, 50% of spontaneously expelled abortuses have been thought to be chromosomally abnormal; about 60…
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2000
2000
Cytogenetics, Immunostaining for Fibroblast Growth Factors, p53 Sequencing, and Clinical Features of Two Cases of Cystosarcoma Phyllodes
P. Woolley
,
S. Gollin
,
+6 authors
Robert Mckenna
Molecular diagnosis (Print)
2000
Corpus ID: 1788987
AbstractBackground: We present cytogenetics and fibroblast growth factor immunohistochemistry in one case of cystosarcoma…
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1997
1997
Clonal identification of trisomies 3, 5 and X in angioimmunoblastic lymphadenopathy with dysproteinemia by fluorescence in situ hybridization.
T. Kumaravel
,
Kimio Tanaka
,
+5 authors
N. Kamada
Leukemia and Lymphoma
1997
Corpus ID: 20501069
Trisomies 3, 5 and X in six Japanese patients with AILD were detected by fluorescence in situ hybridization (FISH). Trisomies 3…
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1989
1989
Trisomy 5 mosaicism in amniotic fluid with normal outcome
A. C. Casamassima
,
P. Wilmot
,
M. Mahoney
,
Robin V. Scott
,
L. Shapiro
Clinical Genetics
1989
Corpus ID: 43101934
A case of prenatally diagnosed true mosaicism for trisomy 5 with a clinically normal outcome is presented. Trisomy 5 was detected…
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1987
1987
Prenatal detection of trisomy 5 mosaicism with normal outcome
K. Richkind
,
R. Apostol
,
S. Puck
Prenatal Diagnosis
1987
Corpus ID: 39024563
Chromosome analysis from genetic amniocentesis occasionally results in mosaicism, making interpretation difficult. A recent issue…
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Review
1987
Review
1987
Chromosome abnormalities in malignant lymphoma in patients from Saitama.
N. Maseki
,
Y. Kaneko
,
+4 authors
S. Takayama
Cancer Research
1987
Corpus ID: 12989335
Clonal chromosome abnormalities were found in 89 (97%) of 92 patients with non-Hodgkin's malignant lymphoma including…
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1981
1981
[Partial monosomy and trisomy 5 p due to balanced translocation t (3,5) in the father (author's transl)].
M. Andrle
,
A. Erlach
,
A. Rett
Wiener Klinische Wochenschrift
1981
Corpus ID: 19930261
A family with three retarded children is described. The phenotypical features of the eldest girl are uncharacteristic, whereas…
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