(Q34461621)

English

Linkage analysis of two families with X-linked recessive congenital motor nystagmus

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Linkage analysis of two families with X-linked recessive congenital motor nystagmus (English)

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Europe PubMed Central

PubMed publication ID

2 August 2017

congenital disorder

0 references

author name string

Xiangming Guo

1

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Shiqiang Li

2

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Xiaoyun Jia

3

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Xueshan Xiao

4

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Panfeng Wang

5

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Qingjiong Zhang

6

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

publication date

21 October 2005

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Journal of Human Genetics

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Europe PubMed Central

PubMed publication ID

2 August 2017

51

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

76-80

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

https://scigraph.springernature.com/pub.10.1007/s10038-005-0316-y

0 references

Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16240070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel association of RP1 gene mutations with autosomal recessive retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/16240070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/16240070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Avoiding recomputation in linkage analysis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16240070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Standard for clinical electroretinography. International Standardization Committee

1 reference

https://pubmed.ncbi.nlm.nih.gov/16240070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Easy calculations of lod scores and genetic risks on small computers

1 reference

https://pubmed.ncbi.nlm.nih.gov/16240070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Confirmation and refinement of a genetic locus of congenital motor nystagmus in Xq26.3-q27.1 in a Chinese family

1 reference

https://pubmed.ncbi.nlm.nih.gov/16240070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/16240070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3

1 reference

https://pubmed.ncbi.nlm.nih.gov/16240070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16240070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Gene for Autosomal Dominant Congenital Nystagmus Localizes to 6p12

1 reference

https://pubmed.ncbi.nlm.nih.gov/16240070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16240070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/16240070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital motor nystagmus linked to Xq26-q27.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16240070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal recessive familial exudative vitreoretinopathy is associated with mutations in LRP5.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16240070

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-005-0316-Y

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

ResearchGate publication ID

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