(Q41278990)

29 September 2017

title

Molecular genetic analysis of tumors in von Recklinghausen neurofibromatosis: loss of heterozygosity for chromosome 17. (English)

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29 September 2017

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Skuse GR

1

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29 September 2017

Kosciolek BA

series ordinal

2

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29 September 2017

Rowley PT

series ordinal

3

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29 September 2017

publication date

1 September 1989

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Genes, Chromosomes and Cancer

29 September 2017

published in

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29 September 2017

volume

1

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29 September 2017

issue

1

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29 September 2017

page(s)

36-41

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Reduction to homozygosity of genes on chromosome 11 in human breast neoplasia

29 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

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A general theory of carcinogenesis

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

Homozygosity of chromosome 13 in retinoblastoma

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

Genetic analysis of NF1: identification of close flanking markers on chromosome 17.

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

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

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

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

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

Suppression of Malignancy by Cell Fusion

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

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Mutation and cancer: statistical study of retinoblastoma

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

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

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

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

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

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

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

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

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

Long-term follow-up of von Recklinghausen neurofibromatosis. Survival and malignant neoplasms

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

Detection of specific sequences among DNA fragments separated by gel electrophoresis

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

Human cell hybrids: analysis of transformation and tumorigenicity

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https://api.crossref.org/works/10.1002%2FGCC.2870010107

7 January 2021

Identifiers

DOI

10.1002/GCC.2870010107

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29 September 2017

1 reference