(Q41868795)

13 October 2017

Genetic heterogeneity of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in families with familial adenomatous polyposis (English)

1 reference

13 October 2017

0 references

Hodgson SV

1

1 reference

13 October 2017

Bishop DT

series ordinal

2

1 reference

13 October 2017

Jay B

series ordinal

3

1 reference

13 October 2017

language of work or name

English

0 references

publication date

1 January 1994

1 reference

Journal of Medical Genetics

13 October 2017

1 reference

13 October 2017

31

1 reference

13 October 2017

1

1 reference

13 October 2017

55-58

1 reference

A genetic study of Gardner syndrome and congenital hypertrophy of the retinal pigment epithelium

13 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049600

Congenital hypertrophy of the retinal pigment epithelium as a marker for familial adenomatous polyposis.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049600

Congenital hypertrophy of retinal pigment epithelium: a sign of familial adenomatous polyposis

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049600

Pigmented lesions of the retinal pigment epithelium and familial adenomatous polyposis.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049600

Association of congenital hypertrophy of the retinal pigment epithelium with familial adenomatous polyposis

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049600

Familial polyposis coli: the spectrum of ocular and other extracolonic manifestations

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049600

The UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculations

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049600

Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049600

Hypertrophy of the retinal pigment epithelium associated with Gardner's syndrome

18 August 2018

1 reference

12 December 2020

Prevalence and importance of pigmented ocular fundus lesions in Gardner's syndrome

1 reference

12 December 2020

Hyperpigmented lesions of the retinal pigment epithelium in familial adenomatous polyposis

1 reference

12 December 2020

Histopathological features of congenital fundus lesions in familial adenomatous polyposis

1 reference

12 December 2020

A clinicopathologic study of the eyes in familial adenomatous polyposis with extracolonic manifestations (Gardner's syndrome)

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.31.1.55

1 reference

13 October 2017

1 reference

13 October 2017

PubMed publication ID

8151639

1 reference