Severe combined immunodeficiency caused by deficiency in either the δ or the ε subunit of CD3

le Basile, Geneviève de Saint, Geissmann, Frédéric, Flori, Elisabeth, Uring-Lambert, Béatrice, Soudais, Claire, Cavazzana-Calvo, Marina, Durandy, Anne, Jabado, Nada, Fischer, Alain, Deist, Françoise Le
Foilsithe 2004

Partial T and B lymphocyte immunodeficiency and predisposition to lymphoma in patients with hypomorphic mutations in Artemis

le Moshous, Despina, Pannetier, Christophe, Chasseval, Régina de, Deist, Françoise le, Cavazzana-Calvo, Marina, Romana, Serge, Macintyre, Elizabeth, Canioni, Danielle, Brousse, Nicole, Fischer, Alain, Casanova, Jean-Laurent, Villartay, Jean-Pierre de
Foilsithe 2003

A Homozygous mucosa-associated ly 1 mphoid tissue 1 (MALT1) mutation in a family with 2 combined immunodeficiency

le Jabara, Haifa H., Ohsumi, Toshiro, Chou, Janet, Massaad, Michel J., Benson, Halli, Megarbane, Andre, Chouery, Eliane, Mikhael, Raymond, Gorka, Oliver, Gewies, Andreas, Portales, Pierre, Nakayama, Toshinori, Hosokawa, Hiroyuki, Revy, Patrick, Herrod, Henry, Deist, Francoise Le, Lefranc, Gerard, Ruland, Jürgen, Geha, Raif S.
Foilsithe 2013

A hypermorphic IκBα mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency

le Courtois, Gilles, Smahi, Asma, Reichenbach, Janine, Döffinger, Rainer, Cancrini, Caterina, Bonnet, Marion, Puel, Anne, Chable-Bessia, Christine, Yamaoka, Shoji, Feinberg, Jacqueline, Dupuis-Girod, Sophie, Bodemer, Christine, Livadiotti, Susanna, Novelli, Francesco, Rossi, Paolo, Fischer, Alain, Israël, Alain, Munnich, Arnold, Deist, Françoise Le, Casanova, Jean-Laurent
Foilsithe 2003