(Q44639901)

4 December 2017

A novel mutation of the growth hormone receptor gene (GHR) in a Chinese girl with Laron syndrome (English)

1 reference

4 December 2017

A Novel Mutation of the Growth Hormone Receptor Gene (GHR) in a Chinese Girl with Laron Syndrome (English)

1 reference

DOI

https://api.crossref.org/works/10.1515/JPEM.2003.16.8.1183

27 March 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14594180

27 March 2024

1 reference

https://api.crossref.org/works/10.1515/JPEM.2003.16.8.1183

27 March 2024

author name string

Xiaoli Chen

1

1 reference

4 December 2017

Fang Song

2

1 reference

4 December 2017

Yaohua Dai

3

1 reference

4 December 2017

Xiulan Bao

4

1 reference

4 December 2017

Yuwei Jin

5

1 reference

4 December 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14594180

27 March 2024

publication date

1 October 2003

1 reference

full work available at URL

4 December 2017

https://www.degruyter.com/document/doi/10.1515/JPEM.2003.16.8.1183/pdf

1 reference

DOI

https://api.crossref.org/works/10.1515/JPEM.2003.16.8.1183

Journal of Pediatric Endocrinology and Metabolism

27 March 2024

published in

1 reference

4 December 2017

16

1 reference

4 December 2017

8

1 reference

4 December 2017

1183-1189

1 reference

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

4 December 2017

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2003.16.8.1183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2003.16.8.1183

Spectrum of growth hormone receptor mutations and associated haplotypes in Laron syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2003.16.8.1183

Growth hormone (GH) insensitivity syndrome with high serum GH-binding protein levels caused by a heterozygous splice site mutation of the GH receptor gene producing a lack of intracellular domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2003.16.8.1183

21 January 2018

Identifiers

DOI

1 reference

release_hqf3iq4bwnes7l5kfcfqn6rjcm

4 December 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/hqf3iq4bwnes7l5kfcfqn6rjcm

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference