(Q48871804)

16 February 2018

title

Loss of heterozygosity on chromosome 22 in human gliomas does not inactivate the neurofibromatosis type 2 gene. (English)

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16 February 2018

neurofibromatosis type II

main subject

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1 reference

7

Rouleau GA

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16 February 2018

4

Rangaratnam S

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16 February 2018

author name string

Watkins D

1

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16 February 2018

Ruttledge MH

2

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16 February 2018

Sarrazin J

3

1 reference

16 February 2018

Poisson M

5

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16 February 2018

Delattre JY

6

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16 February 2018

publication date

1 November 1996

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16 February 2018

Cancer Genetics and Cytogenetics

published in

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16 February 2018

volume

92

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16 February 2018

page(s)

73-78

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16 February 2018

issue

1

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16 February 2018

Loss of heterozygosity for distal markers on 22q in human gliomas

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

A tiger behind many doors: multiple genetic pathways to malignant glioma

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

MTS1/CDKN2 gene mutations are rare in primary human astrocytomas with allelic loss of chromosome 9p

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

Chromosomal patterns in human malignant astrocytomas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

Chromosomal composition of a series of 22 human low-grade gliomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

A cytogenetic study of 53 human gliomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

D22S15--a fetal brain cDNA with BanII and SacI RFLP.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

A genetic linkage map of the long arm of human chromosome 22.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

Isolation and mapping of a polymorphic DNA sequence (pEFZ13) on chromosome 1p [D1S64].

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

RFLP identified by the anonymous DNA segment FZ V D11 at 22q13 [HGM9 no.D22S80]

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

Isolation of anonymous, polymorphic DNA fragments from human chromosome 22q12-qter

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

RFLP detected with a 5'-bcr-gene-sequence (HGM8 provisional no. D22S11).

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

Gamma-glutamyl transferase locus (GGT) displays a PvuII polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

HincII RFLP in the human gene for the heavy neurofilament subunit (NF-H)

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

HindIII polymorphism in the human c-sis proto-oncogene

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

Mapping of human chromosome 22 with a panel of somatic cell hybrids

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

A map of 22 loci on human chromosome 22.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

A panel of human chromosome 22-specific sequence tagged sites

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

Exon scanning for mutation of the NF2 gene in schwannomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

The neurofibromatosis type 2 gene is inactivated in schwannomas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900149-5

7 January 2021

10.1016/S0165-4608(96)00149-5

Identifiers

DOI

1 reference

16 February 2018

release_lmmc32j52ra65moge7s73msjnq

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/lmmc32j52ra65moge7s73msjnq

24 November 2022

mapped directly with Wikidata item

PubMed ID

8956876

1 reference

16 February 2018