X-linked hypohidrotic ectodermal dysplasia and t(X;12) in a female
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1989.tb02973.x/fullpdf
Reference10 articles.
1. Genetic mapping of nine DNA markers in the q11-q12 region of the human X chromosome;Arveiler;Genomics,1987
2. Clinical aspects of X-linked hypohidrotic ectodermal dysplasia;Clarke;Arch. Dis. Child.,1987a
3. X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localization;Clarke;Hum. Genet.,1987b
4. Two human X-autosome translations identified by autoradiography and fluorescence;Cohen;Am. J. Hum. Genet.,1972
5. Genetic mapping of anhidrotic ectodermal dysplasia: DXS 159, a closely linked proximal marker;Hanauer;Hum. Genet.,1988
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1. Genetic analysis of a possible case of canine X‐linked ectodermal dysplasia;Journal of Small Animal Practice;2021-06-02
2. Lésions linéaires : un signe dermatologique clé de la dysplasie ectodermique liée à l’X chez la fille;Annales de Dermatologie et de Vénéréologie;2020-09
3. First report on an X-linked hypohidrotic ectodermal dysplasia family with X chromosome inversion: Breakpoint mapping reveals the pathogenic mechanism and preimplantation genetics diagnosis achieves an unaffected birth;Clinica Chimica Acta;2017-12
4. Chromosomes and the Skin;Harper's Textbook of Pediatric Dermatology;2011-05-24
5. A novel missense mutation (402C → T) in exon 1 in the EDA gene in a family with X-linked hypohidrotic ectodermal dysplasia;Clinical Genetics;2008-06-28
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