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Acquired homozygosity (isodisomy) of chromosome 3 in uveal melanoma
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instance of
scholarly article
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title
Acquired homozygosity (isodisomy) of chromosome 3 in uveal melanoma
(English)
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main subject
uveal melanoma
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based on heuristic
inferred from title
Isodisomy
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based on heuristic
inferred from title
homozygosity
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based on heuristic
inferred from title
author name string
V A White
series ordinal
1
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B K McNeil
series ordinal
2
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D E Horsman
series ordinal
3
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language of work or name
English
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publication date
1 April 1998
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published in
Cancer Genetics and Cytogenetics
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volume
102
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issue
1
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page(s)
40-5
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cites work
Nonrandom chromosomal abnormalities in primary uveal melanoma
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stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Non-random abnormalities of chromosomes 3, 6, and 8 associated with posterior uveal melanoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytogenetic analysis of uveal melanoma. Consistent occurrence of monosomy 3 and trisomy 8q
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytogenetic analysis of posterior uveal melanoma
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stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytogenetic findings in primary uveal melanoma
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytogenetics of twelve cases of uveal melanoma and patterns of nonrandom anomalies and isochromosome formation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A PCR-based genetic map for human chromosome 3
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dinucleotide repeat polymorphism in the human thyroid hormone receptor beta gene (THRB) on chromosome 3.
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
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Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Six dinucleotide microsatellite polymorphisms on human chromosome 3.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frequency and prognostic evaluation of 3p21-22 allelic losses in non-small-cell lung cancer
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
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7 January 2021
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inferred from DOI database lookup
Ordering three DNA polymorphisms on human chromosome 3 by sperm typing
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
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inferred from DOI database lookup
Isolation and characterization of 19 dinucleotide repeat polymorphisms on chromosome 3p.
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reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
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7 January 2021
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inferred from DOI database lookup
Dinucleotide repeat polymorphism in human GLUT2/liver facilitative glucose transporter gene on chromosome 3.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of alleles at polymorphic loci on chromosome 2 in uveal melanoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of chromosome 3 alleles and multiplication of chromosome 8 alleles in uveal melanoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of heterozygosity of the thyroid hormone receptor B in posterior uveal melanoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic imprinting proposed as a surveillance mechanism for chromosome loss
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stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of imprinting in human cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous deletion, rearrangement and hypermethylation implicate chromosome region 3p14.3-3p21.3 in sporadic breast-cancer development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
FHIT gene alterations in head and neck squamous cell carcinomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900290-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0165-4608(97)00290-2
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PubMed publication ID
9530338
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