(Q41735006)

English

Female with hypohidrotic ectodermal dysplasia and de novo (X;9) translocation. Clinical documentation of the AnLy cell line case

scientific article published on May 1990

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

Female with hypohidrotic ectodermal dysplasia and de novo (X;9) translocation. Clinical documentation of the AnLy cell line case (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

hypohidrotic ectodermal dysplasia

1 reference

based on heuristic

inferred from title

author name string

K D MacDermot

1

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

M Hultén

2

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

publication date

1 May 1990

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

84

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

577-579

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localization

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spreading of inactivation in an (X;14) translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two human X-autosome translocations identified by autoradiography and fluorescence

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Follow-up on a human X-autosome translocation first studied in 1963 and 1964

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Banding patterns and autoradiographic studies of cells with an X-autosome translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical aspects of X-linked hypohidrotic ectodermal dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338345

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/2338345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recognition and reanalysis of a cell line from a manifesting female with X linked hypohidrotic ectodermal dysplasia and an X; autosome balanced translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2338345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/2338345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00210814

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 October 2017

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