Cytogenetic and molecular cytogenetic evidence of recurrent 8q24.1 loss in osteochondroma (Q78409549)

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14 December 2019

title

Cytogenetic and molecular cytogenetic evidence of recurrent 8q24.1 loss in osteochondroma (English)

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14 December 2019

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Michael G Feely

1

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14 December 2019

Amber K Boehm

2

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14 December 2019

Robert S Bridge

3

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14 December 2019

Pamela A Krallman

4

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14 December 2019

James R Neff

5

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14 December 2019

Marilu Nelson

6

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14 December 2019

Julia A Bridge

7

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14 December 2019

publication date

1 September 2002

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Cancer Genetics and Cytogenetics

14 December 2019

published in

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14 December 2019

volume

137

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14 December 2019

issue

2

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14 December 2019

page(s)

102-107

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Molecular analysis of overlapping chromosomal deletions in patients with Langer-Giedion syndrome

14 December 2019

cites work

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7 January 2021

A 4-megabase YAC contig that spans the Langer-Giedion syndrome region on human chromosome 8q24.1: use in refining the location of the trichorhinophalangeal syndrome and multiple exostoses genes (TRPS1 and EXT1)

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7 January 2021

Interstitial deletion of 11(p11.2p12): a newly described contiguous gene deletion syndrome involving the gene for hereditary multiple exostoses (EXT2).

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7 January 2021

Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome

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7 January 2021

The natural history of hereditary multiple exostoses

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Cytogenetic and molecular cytogenetic techniques in orthopaedic surgery.

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7 January 2021

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

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7 January 2021

Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses

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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

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7 January 2021

Adamantinoma-like Ewing's sarcoma: genomic confirmation, phenotypic drift

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7 January 2021

Chromosomal abnormalities in low grade chondrosarcoma and a review of the literature

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7 January 2021

Clonal chromosome aberrations with monosomy of chromosome 8 in a case of grade III chondrosarcoma.

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7 January 2021

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

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7 January 2021

Recurrent anomalies of 6q25 in chondromyxoid fibroma.

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7 January 2021

Clonal chromosome abnormalities in enchondromas and chondrosarcomas

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7 January 2021

Chromosome 9 alterations and trisomy 22 in central chondrosarcoma: a cytogenetic and DNA flow cytometric analysis of chondrosarcoma subtypes

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7 January 2021

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

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7 January 2021

An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostoses.

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7 January 2021

Clinical correlation to genetic variations of hereditary multiple exostosis

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7 January 2021

10.1016/S0165-4608(02)00557-5

Identifiers

DOI

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14 December 2019

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