(Q43168499)

15 November 2017

0 references

Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1. (English)

1 reference

15 November 2017

1 reference

Zhang Q

1

1 reference

15 November 2017

Guo X

2

1 reference

15 November 2017

Xiao X

3

1 reference

15 November 2017

Jia X

4

1 reference

15 November 2017

Li S

5

1 reference

15 November 2017

Hejtmancik JF

6

1 reference

15 November 2017

language of work or name

English

0 references

publication date

1 May 2006

1 reference

Journal of Medical Genetics

15 November 2017

1 reference

15 November 2017

43

1 reference

15 November 2017

5

1 reference

15 November 2017

e20

1 reference

Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family.

15 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Refractive error and visual impairment in urban children in southern china.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

A synopsis of the prevalence rates and environmental risk factors for myopia

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Interactions of genes and environment in myopia

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

A new genetic locus for X linked progressive cone-rod dystrophy

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Clinical features and a follow-up study in a family with X-linked progressive cone-rod dystrophy

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

A second locus for familial high myopia maps to chromosome 12q

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Positional cloning of the gene for X-linked retinitis pigmentosa 2

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Evidence that a locus for familial high myopia maps to chromosome 18p

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Prevalence of myopia in the United States

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Prevalence and mode of inheritance of major genetic eye diseases in China.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

X-linked myopia in Danish family.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

X-linked myopia: Bornholm eye disease. Linkage to DNA markers on the distal part of Xq.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy)

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Identification of a novel locus on 2q for autosomal dominant high-grade myopia.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) families

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

X-linked high myopia associated with cone dysfunction.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

A genome wide scan for familial high myopia suggests a novel locus on chromosome 7q36.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Detection of congenital color vision defects using heteroduplex-SSCP analysis.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

Linkage Analysis of the Genetic Loci for High Myopia on 18p, 12q, and 17q in 51 U.K. Families

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564525

The progression of refractive error in school-age children: Shunyi district, China

1 December 2018

1 reference

12 December 2020

A look at slowing progression of myopia

1 reference

12 December 2020

Standard for clinical electroretinography. International Standardization Committee

1 reference

12 December 2020

Genome-wide Scan for Myopia in the Old Order Amish

1 reference

12 December 2020

VISION 2020-the right to sight: from strategies to action

1 reference

12 December 2020

Ocular refraction: heritability and genome-wide search for eye morphometry traits in an isolated Sardinian population

1 reference

12 December 2020

Correlation of gene structure and psychophysical measurement in red-green color vision deficiency in Chinese

1 reference

12 December 2020

New Locus for Autosomal Dominant High Myopia Maps to the Long Arm of Chromosome 17

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.2005.037853

1 reference

15 November 2017

1 reference

15 November 2017

1 reference