(Q67577231)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

title

Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosa (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

1 reference

1 reference

L M Bleeker-Wagemakers

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

A Gal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

R Kumar-Singh

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

L I van den Born

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

Y Li

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

E Schwinger

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

L A Sandkuijl

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

A A Bergen

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

P Kenna

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

P Humphries

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

publication date

1 November 1992

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

volume

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

page(s)

811-812

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

15 September 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980195-8

7 January 2021

A study of retinitis pigmentosa in the City of Birmingham. I Prevalence

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980195-8

7 January 2021

A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980195-8

7 January 2021

On the molecular genetics of retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980195-8

7 January 2021

Autosomal dominant retinitis pigmentosa: a new multi-allelic marker (D3S621) genetically linked to the disease locus (RP4).

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980195-8

7 January 2021

Poly (T/A) polymorphism at the human retinal degeneration slow (RDS) locus

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980195-8

7 January 2021

A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980195-8

7 January 2021

Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2805%2980195-8

7 January 2021

10.1016/S0888-7543(05)80195-8

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1427914%20AND%20SRC:MED&resulttype=core&format=json

15 September 2019

1 reference