(Q34511778)

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12 March 2020

4 references

29 October 2020

14 November 2020

26 January 2021

3 July 2021

Personalized ophthalmology (English)

1 reference

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12 March 2020

5 references

25 April 2019

25 June 2019

19 September 2019

29 October 2020

14 November 2020

biomedical investigative technique

1 reference

19 September 2019

1 reference

29 October 2020

1 reference

14 November 2020

1 reference

26 January 2021

molecular diagnostic techniques

1 reference

3 July 2021

2

1 reference

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12 March 2020

Louise Porter

series ordinal

1

1 reference

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12 March 2020

author name string

L F Porter

series ordinal

1

1 reference

PubMed publication ID

24665880

2 August 2017

publication date

1 July 2014

8 references

25 April 2019

25 June 2019

19 September 2019

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12 March 2020

29 October 2020

14 November 2020

26 January 2021

3 July 2021

8 references

25 April 2019

25 June 2019

19 September 2019

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29 October 2020

14 November 2020

26 January 2021

3 July 2021

86

1 reference

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12 March 2020

issue

1

1 reference

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12 March 2020

page(s)

1-11

1 reference

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Creative Commons Attribution 3.0 Unported

12 March 2020

copyright license

7 references

25 April 2019

25 June 2019

19 September 2019

29 October 2020

14 November 2020

26 January 2021

on focus list of Wikimedia project

3 July 2021

copyright status

copyrighted

0 references

ScienceSource

0 references

cites work

Lake Louise mutation detection meeting 2013: clinical translation of next-generation sequencing requires optimization of workflows and interpretation of variants

1 reference

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Impact of new genomic tools on the practice of clinical genetics in consanguineous populations: the Saudi experience

7 July 2018

1 reference

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A comprehensive review of retinal gene therapy

7 July 2018

1 reference

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Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement

7 July 2018

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Next-generation sequencing in the clinic: promises and challenges

7 July 2018

1 reference

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The future of technologies for personalised medicine

7 July 2018

2 references

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7 July 2018

Genetic insights into age-related macular degeneration: controversies addressing risk, causality, and therapeutics

21 January 2018

1 reference

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The significance of the complement system for the pathogenesis of age-related macular degeneration - current evidence and translation into clinical application

7 July 2018

1 reference

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Genetic counseling and genetic testing in ophthalmology

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4232096

Effect of gene therapy on visual function in Leber's congenital amaurosis

7 July 2018

1 reference

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Initial sequencing and analysis of the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4232096

A paradigm shift in the delivery of services for diagnosis of inherited retinal disease

7 July 2018

1 reference

Genetic testing for inherited eye disease: who benefits?

21 January 2018

1 reference

Genetic influences on the outcome of anti-vascular endothelial growth factor treatment in neovascular age-related macular degeneration

21 January 2018

1 reference

Recommendations for Genetic Testing of Inherited Eye Diseases

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/CGE.12389

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24665880%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

1 reference

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12 March 2020

PubMed publication ID

24665880

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24665880%20AND%20SRC:MED&resulttype=core&format=json