(Q50784187)

English

A new case with 10q23 interstitial deletion encompassing both PTEN and BMPR1A narrows the genetic region deleted in juvenile polyposis syndrome.

scientific article published on 21 September 2012

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22993021

A new case with 10q23 interstitial deletion encompassing both PTEN and BMPR1A narrows the genetic region deleted in juvenile polyposis syndrome. (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22993021

1 reference

based on heuristic

inferred from title

Aleksandar J Dimovski

5

object named as

Aleksandar J Dimovski

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22993021

author name string

Marija Hiljadnikova Bajro

1

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22993021

Elena Sukarova-Angelovska

2

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22993021

Jose Adélaïde

3

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22993021

Max Chaffanet

4

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22993021

publication date

21 September 2012

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22993021

Journal of Applied Genetics

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22993021

54

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22993021

1

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22993021

43-47

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22993021

https://scigraph.springernature.com/pub.10.1007/s13353-012-0115-z

0 references

Integrated profiling of basal and luminal breast cancers.

1 reference

https://api.crossref.org/works/10.1007%2FS13353-012-0115-Z

21 January 2018

High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS13353-012-0115-Z

21 January 2018

PTEN hamartoma tumor syndromes.

1 reference

https://api.crossref.org/works/10.1007%2FS13353-012-0115-Z

21 January 2018

Contribution of PTEN large rearrangements in Cowden disease: a multiplex amplifiable probe hybridisation (MAPH) screening approach.

1 reference

https://api.crossref.org/works/10.1007%2FS13353-012-0115-Z

21 January 2018

Juvenile polyposis and other intestinal polyposis syndromes with microdeletions of chromosome 10q22-23

1 reference

https://api.crossref.org/works/10.1007%2FS13353-012-0115-Z

21 January 2018

Contiguous gene deletion within chromosome arm 10q is associated with juvenile polyposis of infancy, reflecting cooperation between the BMPR1A and PTEN tumor-suppressor genes

1 reference

https://api.crossref.org/works/10.1007%2FS13353-012-0115-Z

21 January 2018

Del(10)(q22.3q24.1) associated with juvenile polyposis.

1 reference

https://api.crossref.org/works/10.1007%2FS13353-012-0115-Z

21 January 2018

Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriers

1 reference

https://api.crossref.org/works/10.1007%2FS13353-012-0115-Z

21 January 2018

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS13353-012-0115-Z

21 January 2018

Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation

1 reference

https://api.crossref.org/works/10.1007%2FS13353-012-0115-Z

21 January 2018

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS13353-012-0115-Z

21 January 2018

Deletion of PTEN and BMPR1A on chromosome 10q23 is not always associated with juvenile polyposis of infancy.

1 reference

https://api.crossref.org/works/10.1007%2FS13353-012-0115-Z

21 January 2018

Reply to Salviati et al.

1 reference

https://api.crossref.org/works/10.1007%2FS13353-012-0115-Z

21 January 2018

Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FS13353-012-0115-Z

21 January 2018

Localization of the Bannayan-Riley-Ruvalcaba syndrome gene to chromosome 10q23.

1 reference

https://api.crossref.org/works/10.1007%2FS13353-012-0115-Z

21 January 2018

Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/22993021

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22993021

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S13353-012-0115-Z

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22993021

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 March 2018

http://europepmc.org/abstract/MED/22993021

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q50784187&oldid=1754432866"