Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: evidence for common founders and independent mutations.
about
A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-prone familiesLocalization of multiple melanoma tumor-suppressor genes on chromosome 11 by use of homozygosity mapping-of-deletions analysis.A locus linked to p16 modifies melanoma risk in Dutch familial atypical multiple mole melanoma (FAMMM) syndrome families.CDKNA2A mutation analysis, protein expression, and deletion mapping of chromosome 9p in conventional clear-cell renal carcinomas: evidence for a second tumor suppressor gene proximal to CDKN2A.A common founder for the V126D CDKN2A mutation in seven North American melanoma-prone families.MELPREDICT: a logistic regression model to estimate CDKN2A carrier probability
P2860
Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: evidence for common founders and independent mutations.
description
1998 nî lūn-bûn
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1998年の論文
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1998年学术文章
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1998年学术文章
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1998年学术文章
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1998年学术文章
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1998年學術文章
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name
Haplotype analysis of two recu ...... ers and independent mutations.
@en
Haplotype analysis of two recu ...... ers and independent mutations.
@nl
type
label
Haplotype analysis of two recu ...... ers and independent mutations.
@en
Haplotype analysis of two recu ...... ers and independent mutations.
@nl
prefLabel
Haplotype analysis of two recu ...... ers and independent mutations.
@en
Haplotype analysis of two recu ...... ers and independent mutations.
@nl
P2093
P1433
P1476
Haplotype analysis of two recu ...... ers and independent mutations.
@en
P2093
A M Goldstein
J Fountain
J Newton-Bishop
M A Tucker
N K Hayward
P A van der Velden
P M Pollock
R Barnhill
P304
P356
10.1002/(SICI)1098-1004(1998)11:6<424::AID-HUMU2>3.3.CO;2-U
P577
1998-01-01T00:00:00Z