(Q37452605)

20 August 2017

Molecular characterization of retinitis pigmentosa in Saudi Arabia (English)

1 reference

20 August 2017

1 reference

1 reference

15

Fowzan S Alkuraya

1 reference

20 August 2017

1

Mohammed A Aldahmesh

1 reference

20 August 2017

8

Arif O Khan

1 reference

20 August 2017

Leen Abu Safieh

2

1 reference

20 August 2017

Hisham Alkuraya

3

1 reference

20 August 2017

Ali Al-Rajhi

4

1 reference

20 August 2017

Hanan Shamseldin

5

1 reference

20 August 2017

Mais Hashem

6

1 reference

20 August 2017

Fatemah Alzahrani

7

1 reference

20 August 2017

Faisal Alqahtani

9

1 reference

20 August 2017

Zuhair Rahbeeni

10

1 reference

20 August 2017

Mohammed Alowain

11

1 reference

20 August 2017

Hanif Khalak

12

1 reference

20 August 2017

Salwa Al-Hazzaa

13

1 reference

20 August 2017

Brian F Meyer

14

1 reference

20 August 2017

24 November 2009

1 reference

20 August 2017

1 reference

20 August 2017

15

1 reference

20 August 2017

2464-2469

1 reference

Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectors

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

Mutation survey of known LCA genes and loci in the Saudi Arabian population

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

Progressive morphological and functional defects in retinas from alpha1 integrin-null mice

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

easyLINKAGE-Plus--automated linkage analyses using large-scale SNP data

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

Genetic diversity among the Arabs

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

Science and society: genetic counselling and customary consanguineous marriage

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

Retinitis pigmentosa: defined from a molecular point of view

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunction

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

Consanguinity and major genetic disorders in Saudi children: a community-based cross-sectional study.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

Age at onset curves of retinitis pigmentosa.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2786884

Allelic heterogeneity in inbred populations: the Saudi experience with Alström syndrome as an illustrative example

2 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19956407

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Differential diagnosis of hereditary pigmentary maculopathies

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19956407

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

20 August 2017

PubMed publication ID

19956407

1 reference