(Q52026513)

English

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

scientific article published in May 1994

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scholarly article

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/8075632

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

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/8075632

Bardet-Biedl syndrome

1 reference

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author name string

Leppert M

1

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/8075632

Baird L

2

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/8075632

Anderson KL

3

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/8075632

Otterud B

4

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/8075632

Lupski JR

5

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/8075632

Lewis RA

6

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/8075632

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publication date

1 May 1994

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/8075632

Nature Genetics

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/8075632

7

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/8075632

1

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/8075632

108-112

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/8075632

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/NG0863-108

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038/NG0863-108

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038/NG0863-108

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038/NG0863-108

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038/NG0863-108

21 January 2018

A second-generation linkage map of the human genome

1 reference

https://api.crossref.org/works/10.1038/NG0863-108

21 January 2018

The Laurence-Moon-Biedl syndrome

1 reference

https://api.crossref.org/works/10.1038/NG0863-108

7 January 2021

based on heuristic

inferred from DOI database lookup

Deafness and the Laurence-Moon-Biedl syndrome

1 reference

https://api.crossref.org/works/10.1038/NG0863-108

7 January 2021

based on heuristic

inferred from DOI database lookup

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/NG0863-108

7 January 2021

based on heuristic

inferred from DOI database lookup

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/NG0863-108

7 January 2021

based on heuristic

inferred from DOI database lookup

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/NG0863-108

7 January 2021

based on heuristic

inferred from DOI database lookup

Linkage analysis and family classification under heterogeneity

1 reference

https://api.crossref.org/works/10.1038/NG0863-108

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/NG0863-108

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/8075632

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/8075632

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