(Q51149294)

English

Refinement of the locus for autosomal recessive cone-rod dystrophy (CORD8) linked to chromosome 1q23-q24 in a Pakistani family and exclusion of candidate genes.

scientific article published on 3 August 2006

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scholarly article

1 reference

Europe PubMed Central

31 March 2018

http://europepmc.org/abstract/MED/16897189

Refinement of the locus for autosomal recessive cone-rod dystrophy (CORD8) linked to chromosome 1q23-q24 in a Pakistani family and exclusion of candidate genes. (English)

1 reference

Europe PubMed Central

31 March 2018

http://europepmc.org/abstract/MED/16897189

1 reference

based on heuristic

inferred from title

cone-rod dystrophy

1 reference

based on heuristic

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author name string

Muhammad Ismail

1

1 reference

Europe PubMed Central

31 March 2018

http://europepmc.org/abstract/MED/16897189

Aiysha Abid

2

1 reference

Europe PubMed Central

31 March 2018

http://europepmc.org/abstract/MED/16897189

Khalid Anwar

3

1 reference

Europe PubMed Central

31 March 2018

http://europepmc.org/abstract/MED/16897189

S Qasim Mehdi

4

1 reference

Europe PubMed Central

31 March 2018

http://europepmc.org/abstract/MED/16897189

Shagufta Khaliq

5

1 reference

Europe PubMed Central

31 March 2018

http://europepmc.org/abstract/MED/16897189

publication date

3 August 2006

1 reference

Europe PubMed Central

31 March 2018

http://europepmc.org/abstract/MED/16897189

Journal of Human Genetics

1 reference

Europe PubMed Central

31 March 2018

http://europepmc.org/abstract/MED/16897189

51

1 reference

Europe PubMed Central

31 March 2018

http://europepmc.org/abstract/MED/16897189

9

1 reference

Europe PubMed Central

31 March 2018

http://europepmc.org/abstract/MED/16897189

827-831

1 reference

Europe PubMed Central

31 March 2018

http://europepmc.org/abstract/MED/16897189

https://scigraph.springernature.com/pub.10.1007/s10038-006-0028-y

0 references

Progressive cone-rod degeneration

1 reference

https://api.crossref.org/works/10.1007%2FS10038-006-0028-Y

21 January 2018

Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Asn244His mutation of the peripherin/RDS gene causing autosomal dominant cone-rod degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RP cone-rod degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CNGA3 mutations in hereditary cone photoreceptor disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence of RPGRIP1 gene mutations associated with recessive cone-rod dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion mapping of a retinal cone-rod dystrophy: assignment to 18q211.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cone and cone-rod dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene for autosomal dominant progressive cone dystrophy (CORD5) maps to chromosome 17p12-p13

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of novel mutations in the SEMA4A gene associated with retinal degenerative diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cone-rod retinal dystrophy in a patient with neurofibromatosis type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16897189

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-006-0028-Y

1 reference

Europe PubMed Central

31 March 2018

http://europepmc.org/abstract/MED/16897189

1 reference

Europe PubMed Central

31 March 2018

http://europepmc.org/abstract/MED/16897189

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