Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1) (Q24610755)

Kirk Mykytyn

1

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Alessandro Iannaccone

Alessandro Iannaccone

11

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Samuel G. Jacobson

Samuel G Jacobson

12

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Edwin M. Stone

Edwin M Stone

20

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Leslie G Biesecker

19

Leslie G Biesecker

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Raoul Hennekam

16

Raoul C M Hennekam

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Alan F Wright

14

Alan F Wright

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Val C. Sheffield

21

Val C Sheffield

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Heidi S Haines

6

Heidi L Haines

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Darryl Y Nishimura

2

Darryl Y Nishimura

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Alberto S Cornier

7

Alberto S Cornier

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Rivka Carmi

10

Rivka Carmi

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Richard G Weleber

13

Richard G Weleber

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Güven Lüleci

17

Güven Lüleci

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author name string

Gretel Beck

4

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Kevin Bugge

5

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Gerald F Cox

8

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Anne B Fulton

9

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Ruth Riise

15

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Sibel Berker-Karauzum

American Journal of Human Genetics

18

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language of work or name

English

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publication date

February 2003

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published in

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volume

72

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issue

2

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page(s)

429-37

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cites work

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A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31

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Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)

7 April 2017

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Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping

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The phenotype in Norwegian patients with Bardet-Biedl syndrome with mutations in the BBS4 gene

7 April 2017

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Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome

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Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome

27 September 2017

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Cardiac abnormalities in the Bardet-Biedl syndrome: echocardiographic studies of 22 patients

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

27 September 2017

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

27 September 2017

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