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Items where Author is "Sprecher, Eli"

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Jump to: 2011 | 2008
Number of items: 3.

2011

Nousbeck, Janna and Burger, Bettina and Fuchs-Telem, Dana and Pavlovsky, Mor and Fenig, Shlomit and Sarig, Ofer and Itin, Peter and Sprecher, Eli. (2011) A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia. American journal of human genetics, Vol. 89, H. 2. pp. 302-307.

Burger, Bettina and Fuchs, Dana and Sprecher, Eli and Itin, Peter. (2011) The immigration delay disease : adermatoglyphia-inherited absence of epidermal ridges. Journal of the American Academy of Dermatology, Vol. 64, H. 5. pp. 974-980.

2008

Lugassy, Jennie and McGrath, John A. and Itin, Peter and Shemer, Revital and Verbov, Julian and Murphy, Helen R. and Ishida-Yamamoto, Akemi and Digiovanna, John J. and Bercovich, Dani and Karin, Nathan and Vitenshtein, Alon and Uitto, Jouni and Bergman, Reuven and Richard, Gabriele and Sprecher, Eli. (2008) KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndrome. Journal of investigative dermatology, Vol. 128, no. 6. pp. 1517-1524.

This list was generated on Wed Apr 1 14:14:22 2020 CEST.