(Q52026513)

20 April 2018

title

Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous. (English)

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20 April 2018

main subject

Bardet-Biedl syndrome

1 reference

Leppert M

1

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20 April 2018

Baird L

2

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20 April 2018

Anderson KL

3

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20 April 2018

Otterud B

4

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20 April 2018

Lupski JR

5

1 reference

20 April 2018

Lewis RA

6

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20 April 2018

language of work or name

English

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publication date

1 May 1994

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20 April 2018

published in

Nature Genetics

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20 April 2018

volume

7

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20 April 2018

issue

1

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20 April 2018

page(s)

108-112

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20 April 2018

https://scigraph.springernature.com/pub.10.1038/ng0594-108

exact match

0 references

cites work

The syndrome of Laurence-Moon-Bardet-Biedl and allied diseases in Switzerland. Clinical, genetic and epidemiological studies

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-108

Laurence-Moon-Biedl syndrome. Report of two unrelated children less than 3 years of age.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-108

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-108

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-108

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-108

A second-generation linkage map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-108

The Laurence-Moon-Biedl syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-108

7 January 2021

Deafness and the Laurence-Moon-Biedl syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-108

7 January 2021

Cloning of the CDNA for a novel photoreceptor membrane protein (rom-1) identifies a disk rim protein family implicated in human retinopathies

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-108

7 January 2021

Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-108

7 January 2021

A minisatellite and a microsatellite polymorphism within 1.5 kb at the human muscle glycogen phosphorylase (PYGM) locus can be amplified by PCR and have combined informativeness of PIC 0.95

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-108

7 January 2021

Linkage analysis and family classification under heterogeneity

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-108

7 January 2021

Identifiers

DOI

10.1038/NG0594-108

1 reference

20 April 2018

1 reference

20 April 2018