(Q33636193)

28 July 2017

title

Molecular basis of human growth hormone gene deletions (English)

1 reference

28 July 2017

C L Vnencak-Jones

1

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28 July 2017

J A Phillips

series ordinal

2

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28 July 2017

E Y Chen

series ordinal

3

1 reference

28 July 2017

P H Seeburg

series ordinal

4

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28 July 2017

language of work or name

English

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publication date

1 August 1988

1 reference

Proceedings of the National Academy of Sciences of the United States of America

28 July 2017

published in

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28 July 2017

volume

85

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28 July 2017

issue

15

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28 July 2017

page(s)

5615-5619

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Structure and evolution of the growth hormone gene family

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281810

The human growth hormone gene family: structure and evolution of the chromosomal locus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281810

Molecular basis for familial isolated growth hormone deficiency

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281810

The genes for growth hormone and chorionic somatomammotropin are on the long arm of human chromosome 17 in region q21 to qter

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281810

The deletion in a type of δ0-β0-thalassaemia begins in an inverted AluI repeat

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281810

Supercoil sequencing: a fast and simple method for sequencing plasmid DNA

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281810

Duplication of seven exons in LDL receptor gene caused by Alu-Alu recombination in a subject with familial hypercholesterolemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281810

Mutation in LDL receptor: Alu-Alu recombination deletes exons encoding transmembrane and cytoplasmic domains

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281810

The human growth hormone gene locus: structure, evolution, and allelic variations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281810

Exon-Alu recombination deletes 5 kilobases from the low density lipoprotein receptor gene, producing a null phenotype in familial hypercholesterolemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281810

Human growth hormone gene deletion without antibody formation or growth arrest during treatment--a new disease entity?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281810

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281810

A gene deletion ending at the midpoint of a repetitive DNA sequence in one form of hereditary persistence of fetal haemoglobin

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281810

Oncogene chromosome breakpoints and alu sequences

30 October 2018

1 reference

12 December 2020

Isolated growth hormone (GH) deficiency type 1A associated with a double deletion in the human GH gene cluster

1 reference

12 December 2020

Familial growth hormone deficiency resulting from a 7.6 kb deletion within the growth hormone gene cluster

1 reference

12 December 2020

A gene deletion is responsible for absence of human chorionic somatomammotropin

1 reference

12 December 2020

An effect of gene dosage on production of human chorionic somatomammotropin

1 reference

12 December 2020

Alpha zero-thalassemia due to recombination between the alpha 1-globin gene and an AluI repeat

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.85.15.5615

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28 July 2017

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28 July 2017

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