(Q54754246)

3 June 2018

title

Loss of constitutional heterozygosity in colon carcinoma from patients with familial polyposis coli. (English)

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3 June 2018

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Okamoto M

1

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3 June 2018

Sasaki M

2

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3 June 2018

Sugio K

3

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3 June 2018

Sato C

4

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3 June 2018

Iwama T

5

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3 June 2018

Ikeuchi T

6

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3 June 2018

Tonomura A

7

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3 June 2018

Sasazuki T

8

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3 June 2018

Miyaki M

9

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3 June 2018

language of work or name

English

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publication date

1 January 1988

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3 June 2018

published in

Nature

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3 June 2018

volume

331

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3 June 2018

issue

6153

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3 June 2018

page(s)

273-277

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3 June 2018

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

cites work

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7 January 2021

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

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7 January 2021

Human retinoblastoma susceptibility gene: cloning, identification, and sequence

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7 January 2021

Structural evidence for the authenticity of the human retinoblastoma gene

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7 January 2021

Cancer biology: Recessive mutation in aetiology of Wilms' tumour

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7 January 2021

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

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7 January 2021

Loss of genes on the short arm of chromosome 11 in bladder cancer

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7 January 2021

Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma

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7 January 2021

Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis

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7 January 2021

Molecular genetic approach to human meningioma: loss of genes on chromosome 22

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7 January 2021

Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma

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7 January 2021

Differential genetic susceptibility of cultured human skin fibroblasts to transformation by Kirsten murine sarcoma virus

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7 January 2021

Localization of the gene for familial adenomatous polyposis on chromosome 5.

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7 January 2021

Chromosome 5 allele loss in human colorectal carcinomas

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7 January 2021

Specific chromosome anomalies and predisposition to human breast, renal cell, and colorectal carcinoma

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7 January 2021

Alterations of myc, myb, and rasHa proto-oncogenes in cancers are frequent and show clinical correlation

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7 January 2021

Chromosome abnormalities in meningiomas

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7 January 2021

Cell culture studies on neurofibromatosis (von Recklinghausen). V. Monosomy 22 and other chromosomal anomalies in cultures from peripheral neurofibromas

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7 January 2021

Deletion of genes on chromosome 1 in endocrine neoplasia

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7 January 2021

A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10

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7 January 2021

Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

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7 January 2021

L-myc, a new myc-related gene amplified and expressed in human small cell lung cancer

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7 January 2021

Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

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7 January 2021

McDonough feline sarcoma virus: characterization of the molecularly cloned provirus and its feline oncogene (v-fms)

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7 January 2021

Restriction fragment length polymorphism associated with the pro alpha 2(I) gene of human type I procollagen. Application to a family with an autosomal dominant form of osteogenesis imperfecta

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7 January 2021

Generation of BALB-MuSV and Ha-MuSV by type C virus transduction of homologous transforming genes from different species

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7 January 2021

Complete nucleotide sequences of the T24 human bladder carcinoma oncogene and its normal homologue

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7 January 2021

Molecular cloning and comparative analyses of the genomes of simian sarcoma virus and its associated helper virus

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7 January 2021

Characterization of the supernumerary chromosome in cat eye syndrome

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7 January 2021

Clustered arrangement of immunoglobulin λ constant region genes in man

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7 January 2021

Variable amplification of immunoglobulin λ light-chain genes in human populations

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7 January 2021

Detection of specific sequences among DNA fragments separated by gel electrophoresis

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7 January 2021

Identifiers

DOI

10.1038/331273A0

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3 June 2018

Dimensions Publication ID

1021002726

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3 June 2018