(Q46822788)

English

Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13.

scientific article published in June 1996

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scholarly article

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13. (English)

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

Jean-michel Rozet

2

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

author name string

A Camuzat

1

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

H Dollfus

3

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

S Gerber

4

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

I Perrault

5

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

J Weissenbach

6

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

A Munnich

7

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

J Kaplan

8

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

publication date

1 June 1996

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

97

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

6

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

798-801

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

[Infantile tapeto-retinal degeneration, Leber type, with marbled aspect of periphery of eye fundus]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic heterogeneity of Usher syndrome type 1 in French families.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Keratoconus in congenital diffuse tapetoretinal degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and genetic heterogeneity in retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Leber's congenital amaurosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A second-generation linkage map of the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis and family classification under heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic heterogeneity of Usher syndrome type II

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ON VARIOUS RECESSIVE BIOTYPES OF LEBER'S CONGENITAL AMAUROSIS

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene for Leber's congenital amaurosis maps to chromosome 17p

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Diagnostic and prognostic importance of the electroretinogram in tapetoretinal degeneration with reduction of the visual field and hemeralopia]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 1993-94 Généthon human genetic linkage map

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Classification of congenital and early onset retinitis pigmentosa.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High hyperopia in Leber's congenital amaurosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8641699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S004390050139

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/8641699

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