(Q31158480)

29 June 2017

Isolation of a candidate gene for Norrie disease by positional cloning (English)

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29 June 2017

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7

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29 June 2017

2

Meindl A

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29 June 2017

Berger W

1

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29 June 2017

van de Pol TJ

3

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29 June 2017

Cremers FP

4

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29 June 2017

Ropers HH

5

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29 June 2017

Döerner C

6

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29 June 2017

Bergen AA

8

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29 June 2017

Lebo R

9

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29 June 2017

Warburg M

10

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29 June 2017

language of work or name

English

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publication date

1 June 1992

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29 June 2017

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29 June 2017

1

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29 June 2017

199-203

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29 June 2017

3

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https://scigraph.springernature.com/pub.10.1038/ng0692-199

29 June 2017

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cites work

Cloning of a gene that is rearranged in patients with choroideraemia

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Norrie disease resulting from a gene deletion: clinical features and DNA studies

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Norrie's disease: close linkage with genetic markers from the proximal short arm of the X chromosome

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Further linkage data on Norrie disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Monoamine oxidase deficiency in males with an X chromosome deletion

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Physical fine-mapping of a deletion spanning the Norrie gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Human monoamine oxidase A and B genes map to Xp 11.23 and are deleted in a patient with Norrie disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Microdeletion in the X-chromosome and prenatal diagnosis in a family with Norrie disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Primary vitreoretinal dysplasia resembling Norrie's disease in a female: association with X autosome chromosomal translocation

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

First demonstration of recombination between the gene for Norrie disease and probe L1.28.

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Yeast artificial chromosome libraries containing large inserts from mouse and human DNA

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Derivation of clones from the choroideremia locus by preparative field inversion gel electrophoresis

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Recognition of protein coding regions in DNA sequences

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Complementary DNA sequencing: expressed sequence tags and human genome project

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

https://api.crossref.org/works/10.1038%2FNG0692-199

1 reference

7 January 2021

Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Norrie's disease--differential diagnosis and treatment

1 reference

https://api.crossref.org/works/10.1038%2FNG0692-199

7 January 2021

Identifiers

DOI

10.1038/NG0692-199

1 reference

Dimensions Publication ID

29 June 2017

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