(Q41560998)

3 October 2017

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title

The spectrum of growth-hormone insensitivity (English)

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3 October 2017

Parks JS

1

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3 October 2017

Brown MR

series ordinal

2

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3 October 2017

Faase ME

series ordinal

3

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3 October 2017

language of work or name

English

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publication date

1 July 1997

1 reference

The Journal of Pediatrics

3 October 2017

published in

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3 October 2017

volume

131

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3 October 2017

issue

1 Pt 2

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3 October 2017

page(s)

S45-50

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Absence of serum growth hormone binding protein in patients with growth hormone receptor deficiency (Laron dwarfism).

3 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970011-8

Absence of the plasma growth hormone-binding protein in Laron-type dwarfism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970011-8

Growth hormone receptor and serum binding protein: purification, cloning and expression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970011-8

Characterization of the human growth hormone receptor gene and demonstration of a partial gene deletion in two patients with Laron-type dwarfism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970011-8

Laron dwarfism and mutations of the growth hormone-receptor gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970011-8

Mutation creating a new splice site in the growth hormone receptor genes of 37 Ecuadorean patients with Laron syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970011-8

A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH-binding activity by abolishing receptor homodimerization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970011-8

Mutations of the growth hormone receptor in children with idiopathic short stature. The Growth Hormone Insensitivity Study Group

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970011-8

Defective membrane expression of human growth hormone (GH) receptor causes Laron-type GH insensitivity syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970011-8

Growth curves for Laron syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970011-8

10.1016/S0022-3476(97)70011-8

7 January 2021

Identifiers

DOI

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3 October 2017

1 reference