Publication: Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis
Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis
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Zonana, J., Schinzel, A., Upadhyaya, M., Thomas, N. S. T., Anton-Lamprecht, I., & Harper, P. S. (1990). Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis. American Journal of Medical Genetics, 35, 132–135. https://doi.org/10.1002/ajmg.1320350125
Abstract
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Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia was previously performed by the direct histological analysis of fetal skin obtained by late second trimester fetoscopy. The recent gene mapping of the locus for the disorder to the region of Xq11-21.1 now permits the indirect prenatal diagnosis of the disorder by the method of linkage analysis, based on closely linked marker loci, during the first trimester of pregnancy. We report the prenatal diagnosis of a male fetus with a high probability of the disorder by a linkage
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- Zonana, Jonathan
- Schinzel, Albert
- Upadhyaya, Meena
- Thomas, Nicholas S T
- Anton-Lamprecht, Ingrun
- Harper, Peter S
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Zonana, J., Schinzel, A., Upadhyaya, M., Thomas, N. S. T., Anton-Lamprecht, I., & Harper, P. S. (1990). Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis. American Journal of Medical Genetics, 35, 132–135. https://doi.org/10.1002/ajmg.1320350125
