(Q24540306)

6 July 2017

title

The gene for cherubism maps to chromosome 4p16. (English)

1 reference

6 July 2017

V Tiziani

1

1 reference

6 July 2017

E Reichenberger

2

1 reference

6 July 2017

C L Buzzo

3

1 reference

6 July 2017

S Niazi

4

1 reference

6 July 2017

N Fukai

5

1 reference

6 July 2017

M Stiller

6

1 reference

6 July 2017

H Peters

7

1 reference

6 July 2017

F M Salzano

8

1 reference

6 July 2017

C M Raposo do Amaral

9

1 reference

6 July 2017

B R Olsen

10

1 reference

6 July 2017

language of work or name

English

0 references

publication date

1 July 1999

1 reference

American Journal of Human Genetics

6 July 2017

published in

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6 July 2017

volume

65

1 reference

6 July 2017

issue

1

1 reference

6 July 2017

page(s)

158-166

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Sequential tests for the detection of linkage

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=1378086

Osteoclast differentiation factor is a ligand for osteoprotegerin/osteoclastogenesis-inhibitory factor and is identical to TRANCE/RANKL

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

A homologue of the TNF receptor and its ligand enhance T-cell growth and dendritic-cell function

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Osteoprotegerin: a novel secreted protein involved in the regulation of bone density

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

A comprehensive genetic map of the human genome based on 5,264 microsatellites

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Mapping a gene for Noonan syndrome to the long arm of chromosome 12

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

TRANCE (tumor necrosis factor [TNF]-related activation-induced cytokine), a new TNF family member predominantly expressed in T cells, is a dendritic cell-specific survival factor

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Construction of cosmid contigs and high-resolution restriction mapping of the Huntington disease region of human chromosome 4.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

The Noonan syndrome/cherubism association

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Cherubism involving a mother and daughter: case reports and review of the literature.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Noonan-like/multiple giant cell lesion syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Cherubism: A report of three cases

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Cherubism: diagnosis, treatment, and comparison with central giant cell granulomas and giant cell tumors

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Cherubism, gingival fibromatosis, epilepsy, and mental deficiency (Ramon syndrome) with juvenile rheumatoid arthritis.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378086

Cherubism: report of a case showing regression without treatment

29 November 2018

1 reference

12 December 2020

Gene for autosomal dominant congenital stationary night blindness maps to the same region as the gene for the beta-subunit of the rod photoreceptor cGMP phosphodiesterase (PDEB) in chromosome 4p16.3.

1 reference

12 December 2020

Retinal changes and tumorigenesis in Ramon syndrome: follow-up of a Brazilian family

1 reference

12 December 2020

A common FGFR3 gene mutation is present in achondroplasia but not in hypochondroplasia

1 reference

12 December 2020

Gingival fibromatosis combined with cherubism

1 reference

12 December 2020

1 reference

12 December 2020

Idiopathic tooth extrusion

1 reference

12 December 2020

Cherubism--hereditary fibrous dysplasia of the jaws. Roentgenographic features

1 reference

12 December 2020

[Cherubism: regression of the lesions and spontaneous bone regeneration]

1 reference

12 December 2020

Cherubism. A thumbnail sketch of its diagnosis and a conservative method of treatment

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F302456

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1086/302456

1 reference

6 July 2017

1 reference

6 July 2017

1 reference