(Q69890195)

English

Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12

scientific article published on 01 November 1986

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2877938%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12 (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2877938%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

ectodermal dysplasia

1 reference

based on heuristic

inferred from title

author name string

S Kølvraa

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2877938%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

T A Kruse

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2877938%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

P K Jensen

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2877938%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

K H Linde

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2877938%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

S R Vestergaard

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2877938%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

L Bolund

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2877938%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

publication date

1 November 1986

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2877938%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2877938%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

74

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2877938%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2877938%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

284-287

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2877938%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00282550

0 references

Proceedings: Report of the Committee on the Genetic Constitution of the X Chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization on the human X of DNA segments cloned from flow sorted chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection in Christ-Siemens-Touraine syndrome (X-linked hypohidrotic ectodermal dysplasia)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypohidrotic ectodermal dysplasia. A study of sweat pores in the X-linked form and in a family with probable autosomal recessive inheritance

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A strategy to reveal high-frequency RFLPs along the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene effect in carriers of anhidrotic ectodermal dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An anonymous single copy X-chromosome clone, pTAK8, identifies a frequent RFLP at Xp11-q12(HGM8 no. DXS146).

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic linkage map of the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Value of sweat pores on fingerprints with organic silicium: a method for the detection of female carriers of anhydrotic ectodermal dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

So-called "anhidrotic ectodermal dysplasia"

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of X-linked hypohidrotic ectodermal dysplasia in six males and in their mothers

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of anhydrotic ectodermal dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-mapping in man: evidence against measurable linkage between anhidrotic ectodermal dysplasia and G6PD deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of Close Linkage Between the Locus for Xg and the Locus for Anhidrotic Ectodermal Dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diminished sweat pores in hypohidrotic ectodermal dysplasia: a new method for assessment

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the Committee on the Genetic Constitution of the X and Y Chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sweat pore counts in ectodermal dysplasias

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypodontia and sweat pore counts in detecting carriers of X-linked hypohidrotic ectodermal dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Christ-Siemens-Touraine syndrome—a clinical and genetic analysis of a large Brazilian kindred: I. Affected females

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Christ-Siemens-Touraine syndrome--a clinical and genetic analysis of a large Brazilian kindred: II. Affected males

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of anhidrotic ectodermal dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2877938

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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