(Q24538751)

6 July 2017

title

Mutations in the EXT1 and EXT2 genes in hereditary multiple exostoses (English)

1 reference

hereditary multiple exostoses

6 July 2017

main subject

1 reference

G Mortier

11

0 references

author name string

W Wuyts

1

1 reference

6 July 2017

W Van Hul

2

1 reference

6 July 2017

K De Boulle

3

1 reference

6 July 2017

J Hendrickx

4

1 reference

6 July 2017

E Bakker

5

1 reference

6 July 2017

F Vanhoenacker

6

1 reference

6 July 2017

F Mollica

7

1 reference

6 July 2017

H J Lüdecke

8

1 reference

6 July 2017

B S Sayli

9

1 reference

6 July 2017

U E Pazzaglia

10

1 reference

6 July 2017

B Hamel

12

1 reference

6 July 2017

E U Conrad

13

1 reference

6 July 2017

M Matsushita

14

1 reference

6 July 2017

W H Raskind

15

1 reference

6 July 2017

P J Willems

16

1 reference

6 July 2017

language of work or name

English

0 references

publication date

1 February 1998

1 reference

American Journal of Human Genetics

6 July 2017

published in

1 reference

6 July 2017

volume

62

1 reference

6 July 2017

issue

2

1 reference

6 July 2017

page(s)

346-354

1 reference

Mutation screening of the EXT1 and EXT2 genes in patients with hereditary multiple exostoses

6 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignancies

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

Genetic heterogeneity in families with hereditary multiple exostoses

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

Genomic organization and promoter structure of the human EXT1 gene

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

Positional cloning of a gene involved in hereditary multiple exostoses

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

HEREDITARY MULTIPLE EXOSTOSIS

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

Identification and characterization of a novel member of the EXT gene family, EXTL2.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

Hereditary multiple exostoses: confirmation of linkage to chromosomes 8 and 11.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

The natural history of hereditary multiple exostoses

27 September 2017

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

27 September 2017

https://api.crossref.org/works/10.1086%2F301726

7 January 2021

inferred from DOI database lookup

Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

Hereditary multiple exostoses.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosomes 8 and 11.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer-Giedion syndrome

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376901

Identification of novel mutations in the human EXT1 tumor suppressor gene

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9463333

12 December 2020

inferred from PubMed ID database lookup

New syndrome: Exostoses, anetodermia, brachydactyly

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9463333

12 December 2020

inferred from PubMed ID database lookup

Identification of a third EXT-like gene (EXTL3) belonging to the EXT gene family.

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F301726

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1086/301726

1 reference

OpenCitations bibliographic resource ID

6 July 2017

3105405

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

6 July 2017

1 reference