학술논문
'학술논문'
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1~10
Academic Journal
Piercecchi-Marti, M.D; Liprandi, A; Sigaudy, S; Fredouille, C; Adalian, P; Figarella-Branger, D; Pellissier, J.F
In Forensic Science International 2004 144(1):7-10
Academic Journal
Alanay, Y; Mohnike, K; Nilsson, O; Alves, I; AlSayed, M; Appelman-Dijkstra, NM; Baujat, G; Ben-Omran, T; Breyer, S; Cormier-Daire, V; Gregersen, PA; Guillen-Navarro, E; Hoegler, W; Maghnie, M; Mukherjee, S; Cohen, S; Pimenta, J; Selicorni, A; Semler, JO; Sigaudy, S; Popkov, D; Sabir, I; Noval, S; Sessa, M; Irving, M
Orphanet journal of rare diseases. 18(1):166
Academic Journal
In Archives de pédiatrie 2001 8(7):728-730
Academic Journal
Bennouna-Greene, V; Kremer, S; Stoetzel, C; Christmann, D; Schuster, C; Durand, M; Verloes, A; Sigaudy, S; Holder-Espinasse, M; Godet, J; Brandt, C; Marion, V; Danion, A; Dietemann, J-L; Dollfus, H
Clinical Genetics. Dec 01, 2011 80(6):523-531
Academic Journal
Germanaud, D; Rossi, M; Bussy, G; Gérard, D; Hertz-Pannier, L; Blanchet, P; Dollfus, H; Giuliano, F; Bennouna-Greene, V; Sarda, P; Sigaudy, S; Curie, A; Vincent, M C; Touraine, R; des Portes, V
Clinical Genetics. Mar 01, 2011 79(3):225-235
Academic Journal
Kerr, B; Delrue, M-A; Sigaudy, S; Perveen, R; Marche, M; Burgelin, I; Stef, M; Tang, B; Eden, O B; O’Sullivan, J; De Sandre-Giovannoli, A; Reardon, W; Brewer, C; Bennett, C; Quarell, O; M’Cann, E; Donnai, D; Stewart, F; Hennekam, R; Cavé, H; Verloes, A; Philip, N; Lacombe, D; Levy, N; Arveiler, B; Black, G
JOURNAL OF MEDICAL GENETICS. May 01, 2006 43(5):401-405
Academic Journal
Krahn, M; Julia, S; Sigaudy, S; Liprandi, A; Bernard, R; Gonnet, K; Heuertz, S; Bonaventure, J; Chau, C; Fredouille, C; Levy, N; Philip, N
Clinical Genetics. Dec 01, 2005 68(6):558-560
Academic Journal
Kerr, B; Mucchielli, M L; Sigaudy, S; Fabre, M; Saunier, P; Voelckel, M A; Howard, E; Elles, R; Eden, T O B; Black, G C; Philip, N
Journal of Medical Genetics. Jun 01, 2003 40(6):469-471
Electronic Resource
Gordon, C; Xue, S; Yigit, G; Filali, H; Chen, K; Rosin, N; Yoshiura, K; Oufadem, M; Beck, T; McGowan, R; Magee, A; Altmuller, J; Dion, C; Thiele, H; Gurzau, A; Nurnberg, P; Meschede, D; Muhlbauer, W; Okamoto, N; Varghese, V; Irving, R; Sigaudy, S; Williams, D; Ahmed, F; Bonnard, C; Kei Kong, M; Ratbi, I; Fejjal, N; Fikri, M; Chafai Elalaoui, S; Reigstad, H; Bole-Feysot, C; Nitschke, P; Ragge, N; Levy, N; Tuncbilek, G; Teo, A; Cunningham, M; Sefiani, A; Kayserili, H; Murphy, J; Chatdokmaiprai, C; Hillmer, A; Wattanasirichaigoon, D; Lyonnet, S; Magdinier, F; Javed, A; Blewitt, M; Amiel, J; Wollnik, B; Reversade, B
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development
Academic Journal
Journal of Medical Genetics; Mar1998, Vol. 35 Issue 3, p238-240, 3p, 4 Black and White Photographs
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[AR] Sigaudy, S
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