X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localization
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00284112.pdf
Reference11 articles.
1. Bolund L, Ahrens P, Albertsen H, Jensen PKA, Kruse TA, Kolvraa S (1986) DNA probes for linkage analysis of X-linked diseases: localisation of the disease locus for anhidrotic ectodermal dysplasia. Clin Genet 29:458 (abstr)
2. Clarke A, Sarfarazi M, Thomas NST (1986) Hypohidrotic ectodermal dysplasia: localization to the proximal long arm of the X chromosome. J Med Genet 23:473 (abstr)
3. Filippi G, Rinaldi A, Crisponi G, Daniels GL, Siniscalco M (1979) X-mapping in man: evidence against measurable linkage between anhidrotic ectodermal dysplasia and G6PD deficiency. J Med Genet 16:223?226
4. Gerald PS, Brown JA (1974) Report of the committee on the genetic constitution of the X chromosome. Cytogenet Cell Genet 13:29?34
5. Kunkel LM, Smith KD, Boyer SH, Borgaonker DS, Wachtel SS, Miller OJ, Breg WR, Jones HW, Rary JM (1977) Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants. Proc Natl Acad Sci USA 74:1245?1249
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