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Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14

Lugassy, J., Itin, P., Ishida-Yamamoto, A., Holland, K.R., Huson, S., Geiger, D., Hennies, Hans C., Indelman, M., Bercovich, D., Uitto, J., Bergman, R., McGrath, J.A., Richard, G. and Sprecher, E. (2006) Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14. American Journal of Human Genetics, 79 (4). pp. 724-730. ISSN 1537-6605

Metadata only available from this repository.
Item Type: Article
Additional Information: Unmapped bibliographic data: ST - Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14 [Field not mapped to EPrints] LB - 14 [Field not mapped to EPrints] RP - Not in File [Field not mapped to EPrints]
Uncontrolled Keywords: analysis
Subjects: Q Science > QH Natural history > QH301 Biology
Q Science > QH Natural history > QH426 Genetics
Schools: School of Applied Sciences
Depositing User: Hans Hennies
Date Deposited: 06 Jul 2016 13:52
Last Modified: 29 Jul 2016 14:29
URI: http://eprints.hud.ac.uk/id/eprint/28819

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