(Q78726693)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12505252%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

title

Recurring breakpoints of 1p13 approximately p22 in osteochondroma (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12505252%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

1 reference

Jeffrey R Sawyer

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12505252%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

Edward L Thomas

2

1 reference

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16 December 2019

Janet L Lukacs

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12505252%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

Charles M Swanson

4

1 reference

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16 December 2019

Yiling Ding

5

1 reference

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16 December 2019

David M Parham

6

1 reference

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16 December 2019

James R Thomas

7

1 reference

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16 December 2019

Richard W Nicholas

8

1 reference

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16 December 2019

publication date

1 October 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12505252%20AND%20SRC:MED&resulttype=core&format=json

Cancer Genetics and Cytogenetics

16 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12505252%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

volume

138

1 reference

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16 December 2019

issue

2

1 reference

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16 December 2019

page(s)

102-106

1 reference

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EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas.

16 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

Biologic and clinical significance of cytogenetic and molecular cytogenetic abnormalities in benign and malignant cartilaginous lesions

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

Familial interstitial deletion 11(p11.12p12) associated with parietal foramina, brachymicrocephaly, and mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

A gene for hereditary multiple exostoses maps to chromosome 19p.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

Structure, chromosomal location, and expression profile of EXTR1 and EXTR2, new members of the multiple exostoses gene family

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

Refined physical mapping and genomic structure of the EXTL1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

Clonal karyotypic abnormalities of the hereditary multiple exostoses chromosomal loci 8q24.1 (EXT1) and 11p11-12 (EXT2) in patients with sporadic and hereditary osteochondromas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

Evidence of an association between 6q13-21 chromosome aberrations and locally aggressive behavior in patients with cartilage tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

Clonal chromosome abnormalities in a so-called Dupuytren's subungual exostosis

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

Constitutional balanced translocations in patients with solid tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

A recurrent chondromyxoid fibroma with chromosome aberrations ins(5;2)(q13;p21p25) and 2p deletion: a case report

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

Recurrent anomalies of 6q25 in chondromyxoid fibroma.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2802%2900598-8

7 January 2021

10.1016/S0165-4608(02)00598-8

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12505252%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

1 reference