(Q35644251)

English

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

scientific article published on May 1995

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scholarly article

1 reference

Europe PubMed Central

9 August 2017

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

1 reference

Europe PubMed Central

9 August 2017

1 reference

based on heuristic

inferred from title

hereditary multiple exostoses

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

J T Hecht

1

1 reference

Europe PubMed Central

9 August 2017

D Hogue

2

1 reference

Europe PubMed Central

9 August 2017

L C Strong

3

1 reference

Europe PubMed Central

9 August 2017

M F Hansen

4

1 reference

Europe PubMed Central

9 August 2017

S H Blanton

5

1 reference

Europe PubMed Central

9 August 2017

M Wagner

6

1 reference

Europe PubMed Central

9 August 2017

language of work or name

0 references

publication date

1 May 1995

1 reference

Europe PubMed Central

9 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

9 August 2017

56

1 reference

Europe PubMed Central

9 August 2017

5

1 reference

Europe PubMed Central

9 August 2017

1125-1131

1 reference

Europe PubMed Central

9 August 2017

Genetic heterogeneity in families with hereditary multiple exostoses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801450

12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801450

12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801450

12 July 2018

The natural history of hereditary multiple exostoses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801450

12 July 2018

Natural history study of hereditary multiple exostoses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801450

12 July 2018

The 1993-94 Généthon human genetic linkage map

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801450

12 July 2018

Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801450

12 July 2018

Strategies for multilocus linkage analysis in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801450

12 July 2018

The tricho-rhino-phalangeal syndrome with exostoses (or Langer-Giedion syndrome): four additional patients without mental retardation and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801450

12 July 2018

The infrequency of malignant disease in diaphyseal aclasis and neurofibromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801450

12 July 2018

Tricho-rhino-phalangeal syndrome type I with severe mental retardation due to interstitial deletion of 8q23.3-24.13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801450

12 July 2018

Complete association of loss of heterozygosity of chromosomes 13 and 17 in osteosarcoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801450

12 July 2018

Multiple exostoses in a patient with t(8;11)(q24.11;p15.5)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801450

12 July 2018

Allelotype analysis in osteosarcomas: frequent allele loss on 3q, 13q, 17p, and 18q.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801450

12 July 2018

The tricho-rhino-phalangeal syndrome(s): chromosome 8 long arm deletion: is there a shortest region of overlap between reported cases? TRP I and TRP II syndromes: are they separate entities?

1 reference

https://pubmed.ncbi.nlm.nih.gov/7726168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene losses in human tumours

1 reference

https://pubmed.ncbi.nlm.nih.gov/7726168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parental origin of mutations of the retinoblastoma gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/7726168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

First cytogenetic evidence of homozygosity for the retinoblastoma deletion in chromosome 13

1 reference

https://pubmed.ncbi.nlm.nih.gov/7726168

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

9 August 2017

1 reference

Europe PubMed Central

9 August 2017

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