(Q62127822)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22083234%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

title

Mapping of locus for autosomal dominant retinitis pigmentosa on chromosome 6q23 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22083234%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference

1

1 reference

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16 January 2020

Hardeep Pal Singh

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22083234%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

author name string

Subhadra Jalali

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22083234%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

publication date

15 November 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22083234%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22083234%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

volume

131

1 reference

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16 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22083234%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

page(s)

717-723

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22083234%20AND%20SRC:MED&resulttype=core&format=json

easyLINKAGE: a PERL script for easy and automated two-/multi-point linkage analyses

16 January 2020

cites work

1 reference

12 December 2020

Genetic analysis of Indian families with autosomal recessive retinitis pigmentosa by homozygosity screening

1 reference

12 December 2020

Retinitis pigmentosa in Spain. The Spanish Multicentric and Multidisciplinary Group for Research into Retinitis Pigmentosa

1 reference

12 December 2020

Homozygous Null Mutations in the ABCA4 Gene in Two Families With Autosomal Recessive Retinal Dystrophy

1 reference

12 December 2020

Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata

1 reference

12 December 2020

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

1 reference

12 December 2020

A genetic analysis of retinitis pigmentosa

1 reference

12 December 2020

Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria

1 reference

12 December 2020

Blindness in the Indian state of Andhra Pradesh

1 reference

12 December 2020

Mutations in known genes account for 58% of autosomal dominant retinitis pigmentosa (adRP).

1 reference

12 December 2020

The molecular basis of human retinal and vitreoretinal diseases

1 reference

12 December 2020

Prevalence of retinitis pigmentosa in Maine

1 reference

12 December 2020

Prevalence of retinitis pigmentosa in urban and rural adult Chinese: The Beijing Eye Study.

1 reference

12 December 2020

Retinitis pigmentosa in southern Africa

1 reference

12 December 2020