(Q35194286)

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Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment.

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8434608%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8434608%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

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hypohidrotic ectodermal dysplasia

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J Zonana

1

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12 October 2019

J Gault

2

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12 October 2019

K J Davies

3

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12 October 2019

M Jones

4

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12 October 2019

D Browne

5

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12 October 2019

M Litt

6

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12 October 2019

N Brockdorff

7

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12 October 2019

S Rastan

8

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12 October 2019

A Clarke

9

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12 October 2019

N S Thomas

10

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12 October 2019

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1 January 1993

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12 October 2019

American Journal of Human Genetics

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12 October 2019

52

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12 October 2019

1

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12 October 2019

78-84

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12 October 2019

Anhidrosis and absence of sweat glands in mice hemizygous for the Tabby gene: supportive evidence for the hypothesis of homology between Tabby and human anhidrotic (hypohidrotic) ectodermal dysplasia (Christ-Siemens-Touraine syndrome).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682116

13 July 2018

X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682116

13 July 2018

A highly polymorphic locus in human DNA revealed by cosmid-derived probes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682116

13 July 2018

Clinical aspects of X-linked hypohidrotic ectodermal dysplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682116

13 July 2018

Construction and analysis of linking libraries from the mouse X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682116

13 July 2018

Clinical and radiographic dental findings in X linked hypohidrotic ectodermal dysplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682116

13 July 2018

Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682116

13 July 2018

Dinucleotide repeat polymorphisms at the DXS453, DXS454 and DXS458 loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682116

13 July 2018

Molecular genetic analysis of the Ta25H deletion: evidence for additional deleted loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682116

13 July 2018

High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682116

13 July 2018

Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682116

27 September 2018

X-linked hypohidrotic ectodermal dysplasia and t(X;12) in a female

1 reference

https://pubmed.ncbi.nlm.nih.gov/8434608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-density molecular map of the central span of the mouse X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8434608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and molecular evidence of an X-chromosome deletion spanning the tabby (Ta) and testicular feminization (Tfm) loci in the mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/8434608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked anhidrotic ectodermal dysplasia and de novo t(X;1) in a female

1 reference

https://pubmed.ncbi.nlm.nih.gov/8434608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8434608%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8434608%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

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