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 November 1986
- journal article
- research article
- Published by Springer Science and Business Media LLC in Human Genetics
- Vol. 74 (3), 284-287
- https://doi.org/10.1007/bf00282550
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- An anonymous single copy X-chromosome clone, pTAK8, identifies a frequent RFLP at Xp11-q12(HGM8 no. DXS146)Nucleic Acids Research, 1986
- The Genetic Linkage Map of the Human X ChromosomeScience, 1985
- A strategy to reveal high-frequency RFLPs along the human X chromosome.1984
- Carrier detection in Christ-Siemens-Touraine syndrome (X-linked hypohidrotic ectodermal dysplasia)1982
- Regional localization on the human X of DNA segments cloned from flow sorted chromosomesNucleic Acids Research, 1982
- [Value of sweat pores on fingerprints with organic silicium: a method for the detection of female carriers of anhydrotic ectodermal dysplasia].1981
- Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.1974
- Report of the Committee on the Genetic Constitution of the X ChromosomeCytogenetic and Genome Research, 1974
- Hypohidrotic ectodermal dysplasia: A study of sweat pores in the X-linked form and in a family with probable autosomal recessive inheritanceThe Journal of Pediatrics, 1971
- Gene effect in carriers of anhidrotic ectodermal dysplasia.Journal of Medical Genetics, 1966