Literature DB >> 4827492

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

P S Gerald, J A Brown.   

Abstract

Mesh：

Year:  1974        PMID： 4827492     DOI： 10.1159/000130228

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


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  16 in total

1.  Autosomal recessive anhidrotic ectodermal dysplasia in a large Moroccan family.

Authors:  K Kabbaj; L Baala; H Chhoul; A Sefiani
Journal:  J Med Genet       Date:  1998-12       Impact factor: 6.318

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

Authors:  J Zonana; A Clarke; M Sarfarazi; N S Thomas; K Roberts; K Marymee; P S Harper
Journal:  Am J Hum Genet       Date:  1988-07       Impact factor: 11.025

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

Authors:  K D MacDermot; R M Winter; S Malcolm
Journal:  Hum Genet       Date:  1986-10       Impact factor: 4.132

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

Authors:  J Zonana; S H Roberts; N S Thomas; P S Harper
Journal:  J Med Genet       Date:  1988-06       Impact factor: 6.318

Review 5.  Hypohidrotic ectodermal dysplasia.

Authors:  A Clarke
Journal:  J Med Genet       Date:  1987-11       Impact factor: 6.318

6.  Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal marker.

Authors:  A Hanauer; Y Alembik; B Arveiler; L Formiga; S Gilgenkrantz; J L Mandel
Journal:  Hum Genet       Date:  1988-10       Impact factor: 4.132

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

Authors:  A Clarke; M Sarfarazi; N S Thomas; K Roberts; P S Harper
Journal:  Hum Genet       Date:  1987-04       Impact factor: 4.132

8.  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.

Authors:  S Kølvraa; T A Kruse; P K Jensen; K H Linde; S R Vestergaard; L Bolund
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

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

Authors:  K D MacDermot; M Hultén
Journal:  Hum Genet       Date:  1990-05       Impact factor: 4.132

10.  Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq.

Authors:  F P Cremers; T J van de Pol; B Wieringa; M H Hofker; P L Pearson; R A Pfeiffer; M Mikkelsen; A Tabor; H H Ropers
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025
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