(Q40850276)

24 September 2017

title

Exclusion of the gastrin-releasing peptide receptor (GRPR) locus as a candidate gene for Rett syndrome (English)

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24 September 2017

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Heidary G

1

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24 September 2017

Hampton LL

2

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24 September 2017

Schanen NC

3

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24 September 2017

Rivkin MJ

4

1 reference

24 September 2017

Darras BT

5

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24 September 2017

Battey J

6

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24 September 2017

Francke U

7

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24 September 2017

publication date

1 June 1998

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American Journal of Medical Genetics Part A

24 September 2017

published in

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24 September 2017

volume

78

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24 September 2017

issue

2

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24 September 2017

page(s)

173-175

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A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes

24 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980630%2978%3A2%3C173%3A%3AAID-AJMG15%3E3.0.CO%3B2-K

Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980630%2978%3A2%3C173%3A%3AAID-AJMG15%3E3.0.CO%3B2-K

Autism, mental retardation, multiple exostoses and short stature in a female with 46,X,t(X;8)(p22.13;q22.1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980630%2978%3A2%3C173%3A%3AAID-AJMG15%3E3.0.CO%3B2-K

WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980630%2978%3A2%3C173%3A%3AAID-AJMG15%3E3.0.CO%3B2-K

Molecular cloning and characterization of receptors for the mammalian bombesin-like peptides

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980630%2978%3A2%3C173%3A%3AAID-AJMG15%3E3.0.CO%3B2-K

Rett's syndrome: prevalence and impact on progressive severe mental retardation in girls

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980630%2978%3A2%3C173%3A%3AAID-AJMG15%3E3.0.CO%3B2-K

Is Rett Syndrome Caused by a Triplet Repeat Expansion?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980630%2978%3A2%3C173%3A%3AAID-AJMG15%3E3.0.CO%3B2-K

Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980630%2978%3A2%3C173%3A%3AAID-AJMG15%3E3.0.CO%3B2-K

Rett phenotype with X/autosome translocation: possible mapping to the short arm of chromosome X.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980630%2978%3A2%3C173%3A%3AAID-AJMG15%3E3.0.CO%3B2-K

Comparative mapping of the Grpr locus on the X chromosomes of man and mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980630%2978%3A2%3C173%3A%3AAID-AJMG15%3E3.0.CO%3B2-K

A new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion map.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980630%2978%3A2%3C173%3A%3AAID-AJMG15%3E3.0.CO%3B2-K

The pathogenicity of the Pro1148Ala substitution in the FBN1 gene: causing or predisposing to Marfan syndrome and aortic aneurysm, or clinically innocent?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980630%2978%3A2%3C173%3A%3AAID-AJMG15%3E3.0.CO%3B2-K

A de novo X;3 translocation in Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980630%2978%3A2%3C173%3A%3AAID-AJMG15%3E3.0.CO%3B2-K

10.1002/(SICI)1096-8628(19980630)78:2<173::AID-AJMG15>3.0.CO;2-K

21 January 2018

Identifiers

DOI

1 reference

24 September 2017

1 reference