(Q39590706)

13 September 2017

title

Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma (English)

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13 September 2017

Gusella JF

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13 September 2017

Seizinger BR

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13 September 2017

Martuza RL

series ordinal

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13 September 2017

language of work or name

English

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publication date

1 August 1986

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13 September 2017

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13 September 2017

volume

322

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13 September 2017

issue

6080

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13 September 2017

page(s)

644-647

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Cellular oncogenes and retroviruses

13 September 2017

cites work

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7 January 2021

Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour

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7 January 2021

Development of homozygosity for chromosome 11p markers in Wilms' tumour

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7 January 2021

Loss of a Harvey ras allele in sporadic Wilms' tumour

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7 January 2021

Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours.

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7 January 2021

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

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7 January 2021

Homozygosity of chromosome 13 in retinoblastoma

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7 January 2021

The descriptive epidemiology of primary intracranial neoplasms: the Connecticut experience

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7 January 2021

Central neurofibromatosis with bilateral acoustic neuroma: genetic, clinical and biochemical distinctions from peripheral neurofibromatosis

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7 January 2021

Cytological and cytogenetical studies on human meningioma

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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

Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition

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7 January 2021

Hereditary Combined Neurinomas and Meningiomas

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7 January 2021

Structural gene for beta-nerve growth factor not defective in familial dysautonomia

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7 January 2021

A polymorphic DNA marker genetically linked to Huntington's disease

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7 January 2021

Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome.

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7 January 2021

Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques

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7 January 2021

A Polymorphic Locus Near the Human Insulin Gene Is Associated with Insulin-dependent Diabetes Melliitus

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7 January 2021

Chromosome 13 restriction fragment length polymorphisms

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7 January 2021

A highly polymorphic locus in human DNA

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7 January 2021

Patterns of polymorphism and linkage disequilibrium suggest independent origins of the human growth hormone gene cluster

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7 January 2021

Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.

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7 January 2021

Cloned DNA probes regionally mapped to human chromosome 21 and their use in determining the origin of nondisjunction

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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

Identifiers

DOI

10.1038/322644A0

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Dimensions Publication ID

13 September 2017

1009770409

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