(Q41669135)

6 October 2017

1 reference

title

Genealogy, natural history, and phenotype of Alström syndrome in a large Acadian kindred and three additional families (English)

1 reference

6 October 2017

1 reference

Marshall JD

1

1 reference

6 October 2017

Ludman MD

2

1 reference

6 October 2017

Shea SE

3

1 reference

6 October 2017

Salisbury SR

4

1 reference

6 October 2017

Willi SM

5

1 reference

6 October 2017

LaRoche RG

6

1 reference

6 October 2017

Nishina PM

7

1 reference

6 October 2017

1 December 1997

1 reference

American Journal of Medical Genetics Part A

6 October 2017

1 reference

6 October 2017

73

1 reference

6 October 2017

150-161

1 reference

6 October 2017

2

1 reference

Laurence, Moon, Bardet, and Biedl: reflections on a syndrome

6 October 2017

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C150%3A%3AAID-AJMG9%3E3.0.CO%3B2-Y

Phenotypic differences among patients with Bardet-Biedl syndrome linked to three different chromosome loci.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C150%3A%3AAID-AJMG9%3E3.0.CO%3B2-Y

Alstrom's syndrome: further evidence of autosomal recessive inheritance and endocrinological dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C150%3A%3AAID-AJMG9%3E3.0.CO%3B2-Y

Homozygosity mapping at Alström syndrome to chromosome 2p

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C150%3A%3AAID-AJMG9%3E3.0.CO%3B2-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C150%3A%3AAID-AJMG9%3E3.0.CO%3B2-Y

Natural history of Alström syndrome in early childhood: onset with dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C150%3A%3AAID-AJMG9%3E3.0.CO%3B2-Y

Impaired insulin-induced RNA synthesis secondary to a genetically defective insulin receptor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C150%3A%3AAID-AJMG9%3E3.0.CO%3B2-Y

The Alström syndrome: ophthalmic histopathology and retinal ultrastructure

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819971212%2973%3A2%3C150%3A%3AAID-AJMG9%3E3.0.CO%3B2-Y

10.1002/(SICI)1096-8628(19971212)73:2<150::AID-AJMG9>3.0.CO;2-Y

21 January 2018

Identifiers

DOI

1 reference

6 October 2017

1 reference