(Q64979604)

2 July 2019

title

Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal marker. (English)

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2 July 2019

Anhidrotic ectodermal dysplasia

main subject

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A Hanauer

1

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2 July 2019

Y Alembik

2

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2 July 2019

B Arveiler

3

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2 July 2019

L Formiga

4

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2 July 2019

S Gilgenkrantz

5

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2 July 2019

J L Mandel

6

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2 July 2019

publication date

1 October 1988

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2 July 2019

published in

Human Genetics

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2 July 2019

volume

80

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2 July 2019

issue

2

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2 July 2019

page(s)

177-180

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2 July 2019

https://scigraph.springernature.com/pub.10.1007/bf00702863

exact match

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cites work

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

1 reference

12 December 2020

Assignment of a structural gene for beta-glucuronidase to human chromosome C7.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Gene effect in carriers of anhidrotic ectodermal dysplasia

1 reference

12 December 2020

Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome

1 reference

12 December 2020

Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletion.

1 reference

12 December 2020

A PstI RFLP detected by probe cpX73 (DXS159) in Xq11-q12.

1 reference

12 December 2020

Manifestation of the lines of Blaschko in women heterozygous for X-linked hypohidrotic ectodermal dysplasia

1 reference

12 December 2020

A Stain for Sweat Pores

1 reference

12 December 2020

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

12 December 2020

Genetic mapping of nine DNA markers in the q11----q22 region of the human X chromosome

1 reference

12 December 2020

Christ-Siemens-Touraine syndrome. Investigations on two large brazilian kindreds with a new estimate of the manifestation rate among carriers

1 reference

12 December 2020

Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation

1 reference

12 December 2020

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

1 reference

12 December 2020

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

1 reference

12 December 2020

Report of the committee on human gene mapping by recombinant DNA techniques

1 reference

12 December 2020

Prenatal diagnosis of anhidrotic ectodermal dysplasia

1 reference

12 December 2020

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

12 December 2020

Identifiers

DOI

10.1007/BF00702863

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2 July 2019

Dimensions Publication ID

1033427626

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2 July 2019