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Autosomal-dominant hypohidrotic ectodermal dysplasia caused by a novel mutation

✍ Scribed by F Valcuende-Cavero; F Martinez; G Pérez-Pastor; S Oltra; I Ferrer; G Tomás-Cabedo; M Moreno-Presmanes


Book ID
111095545
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
610 KB
Volume
22
Category
Article
ISSN
0926-9959

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Autosomal dominant hypohidrotic ectoderm
✍ Aswegan, Andrew L.; Josephson, Kevin D.; Mowbray, Rodney; Pauli, Richard M.; Spr 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 53 KB 👁 2 views

We have studied an autosomal dominant hypohidrotic ectodermal dysplasia in 38 individuals over six generations in one family. Thirty-two affected individuals in four generations are still living. Questionnaire responses were received from 21 of the affected relatives and some of the individuals were