(Q34348965)

1 August 2017

title

Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneity (English)

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1 August 2017

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Bardet-Biedl syndrome

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Kwitek-Black AE

1

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1 August 2017

Carmi R

2

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1 August 2017

Duyk GM

3

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1 August 2017

Buetow KH

4

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1 August 2017

Elbedour K

5

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1 August 2017

Parvari R

6

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1 August 2017

Yandava CN

7

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1 August 2017

Stone EM

8

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1 August 2017

Sheffield VC

9

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1 August 2017

language of work or name

English

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publication date

1 December 1993

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1 August 2017

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1 August 2017

volume

5

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1 August 2017

issue

4

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1 August 2017

page(s)

392-396

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https://scigraph.springernature.com/pub.10.1038/ng1293-392

1 August 2017

exact match

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cites work

The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

Bardet-Biedl syndrome and related disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

Bardet-Biedl and Laurence-Moon syndromes in a mixed Arab population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

The gene for Best's macular dystrophy is located at 11q13 in a Swedish family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

High incidence of Bardet Biedl syndrome among the Bedouin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

7 January 2021

Positional cloning: let's not call it reverse anymore

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

7 January 2021

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

7 January 2021

A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p.

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

7 January 2021

Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

7 January 2021

Localization of Usher syndrome type II to chromosome 1q.

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

7 January 2021

Localization of two genes for Usher syndrome type I to chromosome 11.

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

7 January 2021

Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

7 January 2021

A gene for Usher syndrome type I (USH1A) maps to chromosome 14q

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

7 January 2021

Rhodopsin mutations in autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

7 January 2021

Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

7 January 2021

Obesity, hypertension, and renal disease in relatives of Bardet-Biedl syndrome sibs

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

7 January 2021

A simple and efficient non-organic procedure for the isolation of genomic DNA from blood

1 reference

https://api.crossref.org/works/10.1038%2FNG1293-392

7 January 2021

Identifiers

DOI

10.1038/NG1293-392

1 reference

1 August 2017

1 reference