(Q21198716)

1

Douglas L

Riegert-Johnson

1 reference

19 August 2022

Ferga C Gleeson

2

Ferga C

Gleeson

1 reference

19 August 2022

Maegan Roberts

3

Maegan

Roberts

1 reference

19 August 2022

Krysta Tholen

4

Krysta

Tholen

1 reference

19 August 2022

Lauren Youngborg

5

Lauren

Youngborg

1 reference

19 August 2022

Melvin Bullock

6

Melvin

Bullock

1 reference

19 August 2022

Lisa A Boardman

7

Lisa A

Boardman

1 reference

Hereditary Cancer in Clinical Practice

19 August 2022

language of work or name

English

0 references

publication date

2010

0 references

published in

1 reference

Trichothiodystrophy: a systematic review of 112 published cases characterises a wide spectrum of clinical manifestations

PubMed

volume

8

0 references

issue

1

0 references

page(s)

6

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904729

Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904729

American College of Gastroenterology guidelines for colorectal cancer screening 2009 [corrected]

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904729

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904729

Cowden syndrome: a critical review of the clinical literature

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904729

Frequency and spectrum of cancers in the Peutz-Jeghers syndrome

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904729

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904729

Trichilemmomal carcinoma in a patient with Cowden's disease (multiple hamartoma syndrome).

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904729

Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904729

Testicular mixed germ cell tumor in an adolescent with cowden disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904729

Germline mutations in PTEN are present in Bannayan-Zonana 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=2904729

The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly.

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1897-4287-8-6

Multiple colon carcinomas in a patient with Cowden syndrome.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904729

Screening with magnetic resonance imaging and mammography of a UK population at high familial risk of breast cancer: a prospective multicentre cohort study (MARIBS).

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2904729

Genetic/familial high-risk assessment: breast and ovarian

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20565722

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1897-4287-8-6

1 reference

0 references

1 reference

1 reference

PubMed publication ID

20565722

1 reference