(Q34254893)

31 July 2017

title

Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies (English)

1 reference

31 July 2017

1 reference

3

Whyte MP

1 reference

31 July 2017

Thakker RV

1

1 reference

31 July 2017

Davies KE

series ordinal

2

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31 July 2017

Wooding C

series ordinal

4

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31 July 2017

O'Riordan JL

series ordinal

5

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31 July 2017

language of work or name

English

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publication date

1 July 1990

1 reference

Journal of Clinical Investigation

31 July 2017

published in

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31 July 2017

volume

86

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31 July 2017

issue

1

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31 July 2017

page(s)

40-45

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True idiopathic hypoparathyroidism as a sexlinked recessive trait

31 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=296687

The association of the DiGeorge anomalad with partial monosomy of chromosome 22.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296687

Strategies for multilocus linkage analysis in humans

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296687

Easy calculations of lod scores and genetic risks on small computers

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296687

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296687

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296687

Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in region Xq26?qter

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296687

Guidelines for human gene nomenclature. An international system for human gene nomenclature (ISGN, 1987).

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296687

Exclusion of close linkage between the parathyroid hormone gene and a mutant gene locus causing idiopathic hypoparathyroidism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296687

Familial isolated hypoparathyroidism: a molecular genetic analysis of 8 families with 23 affected persons.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296687

Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296687

Detection of specific sequences among DNA fragments separated by gel electrophoresis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296687

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296687

Complete amino acid sequence of human parathyroid hormone

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296687

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296687

Chronic hypoparathyroidism in two generations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296687

Report of the committee on the genetic constitution of the X and Y chromosomes

28 October 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/1973175

12 December 2020

A deletion in chromosome 22 can cause DiGeorge syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1973175

12 December 2020

Human parathyroid hormone gene (PTH) is on short arm of chromosome 11

1 reference

https://pubmed.ncbi.nlm.nih.gov/1973175

12 December 2020

Absence of parathyroid tissue in sex-linked recessive hypoparathyroidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/1973175

12 December 2020

Familial Idiopathic Hypoparathyroidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/1973175

12 December 2020

Idiopathic hypoparathyroidism presenting with seizures during infancy: X-linked recessive inheritance in a large Missouri kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/1973175

12 December 2020

Familial third-fourth pharyngeal pouch syndrome with apparent autosomal dominant transmission

1 reference

https://pubmed.ncbi.nlm.nih.gov/1973175

12 December 2020

In situ hybridization and translocation breakpoint mapping. III. DiGeorge syndrome with partial monosomy of chromosome 22

1 reference

https://pubmed.ncbi.nlm.nih.gov/1973175

12 December 2020

Identifiers

DOI

10.1172/JCI114712

1 reference

31 July 2017

1 reference

31 July 2017

1 reference