Alopecia Universalis Associated with a Mutation in the Human Hairless Gene by Ahmad, Wasim, Muhammad Faiyaz ul Haque, Brancolini, Valeria, Tsou, Hui C., Haque, Sayed ul, Lam, HaMut, Aita, Vincent M., Owen, Jason, deBlaquiere, Michelle, Frank, Jorge, Cserhalmi-Friedman, Peter B., Leask, Andrew, McGrath, John A., Peacocke, Monica, Ahmad, Mahmud, Ott, Jurg, Christiano, Angela M.

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Trans-gender induction of hair follicles by Jahoda, Colin A. B, Reynolds, Amanda J, Lawrence, Clifford, Cserhalmi-Friedman, Peter B, Christiano, Angela M

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Exposing the human nude phenotype by Frank, Jorge, Pignata, Claudio, Panteleyev, Andrei A, Prowse, David M, Baden, Howard, Weiner, Lorin, Gaetaniello, Lucia, Ahmad, Wasim, Pozzi, Nicola, Cserhalmi-Friedman, Peter B, Aita, Vincent M, Uyttendaele, Hendrik, Gordon, Derek, Ott, Jurg, Brissette, Janice L, Christiano, Angela M

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Paternal germline mosaicism in Herlitz junctional epidermolysis bullosa by Cserhalmi-Friedman, Peter B., Anyane-Yeboa, Kwame, Christiano, Angela M.

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Recapitulation of the hairless mouse phenotype using catalytic oligonucleotides: implications for permanent hair removal by Cserhalmi-Friedman, Peter B., Panteleyev, Andrey A., Christiano, Angela M.

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Germline fumarate hydratase mutations and evidence for a founder mutation underlying multiple cutaneous and uterine leiomyomata by Chuang, Gary S., Martinez-Mir, Amalia, Geyer, Adam, Engler, Danielle E., Glaser, Benjamin, Cserhalmi-Friedman, Peter B., Gordon, Derek, Horev, Liran, Lukash, Barbara, Herman, Eric, Cid, Manuel Prieto, Brenner, Sarah, Landau, Marina, Sprecher, Eli, Garcia Muret, Maria Pilar, Christiano, Angela M., Zlotogorski, Abraham

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Strategy to assess the efficiency of U1 RNA-hammerhead ribozyme constructs using GFP-tagged targets by Cserhalmi-Friedman, Peter B., Djabali, Karima, Dietz, Harry C., Christiano, Angela M.

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Structural Analysis and Mutation Detection Strategy for the Human LamC3 Gene by Cserhalmi-Friedman, Peter B., Olson, Pamela F., Koch, Manuel, Champliaud, Marie-France, Brunken, William J., Burgeson, Robert E., Christiano, Angela M.

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Identification of a glycine substitution and a splice site mutation in the type VII collagen gene in a proband with mitis recessive dystrophic epidermolysis bullosa by CSERHALMI-FRIEDMAN, P. B, KARPATI, S, HORVATH, A, CHRISTIANO, A. M

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Preimplantation genetic diagnosis in a family at risk for recurrence of Herlitz junctional epidermolysis bullosa by Cserhalmi-Friedman, Peter B., Tang, Yaxu, Grifo, Jamie A., Christiano, Angela M.

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