Literature DB >> 469901

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

G Filippi, A Rinaldi, G Crisponi, G L Daniels, M Siniscalco.   

Abstract

A Sardinian kindred segregating for X-linked anhidrotic ectodermal dysplasia (AED), glucose-6-phosphate dehydrogenase (G6PD) deficiency of Mediterranean type, and Xga blood antigen provides evidence against a measurable linkage between the loci for AED and G6PD. Moreover, from the segregation of the combined phenotypes in four scorable sons from two triple heterozygotes with phase known, it seems highly probable that the AED locus is nearer to the centromere than is the G6PD locus.

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Year:  1979        PMID： 469901      PMCID： PMC1012696          DOI： 10.1136/jmg.16.3.223

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


  5 in total

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

Authors:  J A Brown; S Goss; H P Klinger; O J Miller; S Ohno; M Siniscalco
Journal:  Birth Defects Orig Artic Ser       Date:  1976

2.  Studies of Glucose-6-Phosphate Dehydrogenase Activity of Individual Erythrocytes: The Methemoglobin-Elution Test for Identification of Females Heterozygous for G6PD Deficiency.

Authors:  J C Gall; G J Brewer; R J Dern
Journal:  Am J Hum Genet       Date:  1965-07       Impact factor: 11.025

3.  Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia.

Authors:  A Rinaldi; G Filippi; M Siniscalco
Journal:  Am J Hum Genet       Date:  1976-09       Impact factor: 11.025

4.  X chromosome inactivation in X-linked hypohidrotic ectodermal dysplasia.

Authors:  E Passarge; E Fries
Journal:  Nat New Biol       Date:  1973-09-12

5.  Failure to detect linkage between Xg and other X-borne loci in Sardinians.

Authors:  M Siniscalco; G Filippi; B Latte; S Piomelli; M Rattazzi; J Gavin; R Sanger; R R Race
Journal:  Ann Hum Genet       Date:  1966-03       Impact factor: 1.670
  5 in total
  6 in total

Review 1.  Hypohidrotic ectodermal dysplasia.

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

2.  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

3.  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

4.  Further evidence against linkage between Christ-Siemens-Touraine (CST) and XG loci.

Authors:  E A Chautard-Freire-Maia; S L Primo-Parmo; M Pinheiro; N Freire-Maia
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

5.  Ectodermal dysplasia in females and inversion of chromosome 9.

Authors:  H M Fuenmayor; L Roldan-París; H Bermúdez
Journal:  J Med Genet       Date:  1981-06       Impact factor: 6.318

6.  Hypohidrotic ectodermal dysplasia associated with glucose-6-phosphate dehydrogenase deficiency.

Authors:  Aylin Türel Ermertcan; Ali Yaşar; Tuba Çelebı Kayhan; Hüseyin Gülen; Pelin Ertan
Journal:  Ann Dermatol       Date:  2011-09-30       Impact factor: 1.444
  6 in total

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