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	Title	Author(s)	Issue Date
	Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases Journal:Human Mutation	Vegas, N Demir, Z Gordon, CT Breton, S Romanelli Tavares, VL Moisset, H Zechi-Ceide, R Kokitsu-Nakata, NM Kido, Y Marlin, S Gherbi Halem, S Meerschaut, L Callewaert, B Chung, BHY Revencu, N Lehalle, D Petit, F Propst, EJ Papsin, BC Phillips, JH Jakobsen, L Le Tanno, P Thevenon, J McGaughran, J Gerkes, EH Leoni, C Kroisel, P Tan, TY Henderson, A Terhal, P Basel-Salmon, L Alkindy, A White, SM Passos-Bueno, MR Pingault, V De Pontual, L Amiel, J	2022
	MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis Journal:Brain	Mak, CCY Doherty, D Lin, AE Vegas, N Cho, MT Viot, G Dimartino, C Weisfeld-Adams, JD Lessel, D Joss, S Li, C Gonzaga-Jauregui, C Zarate, YA Ehmke, N Horn, D Troyer, C Kant, SG Lee, Y Ishak, GE Leung, G Barone Pritchard, A Yang, S Bend, EG Filippini, F Roadhouse, C Lebrun, N Mehaffey, MG Martin, P-M Apple, B Millan, F Puk, O Hoffer, MJV Henderson, LB McGowan, R Wentzensen, IM Pei, S Zahir, FR YU, M Gibson, WT Senab, A Steeves, M Murrell, JR Luettgen, S Francisco, E Strom, TM Amlie-Wolf, L Kaindl, AM Wilson, WG Halbach, S Basel-Salmon, L Lev-El, N Denecke, J Vissers, LELM Radtke, K Chelly, J Zackai, E Friedman, JM Bamshad, MJ Nickerson, DA Reid, RR Devriendt, K Chae, JH Stolerman, E McDougall, C Powis, Z Bienvenu, T Tan, TY Orenstein, N Dobyns, WB Shieh, JT Choi, M Waggoner, D Gripp, KW Parker, MJ Stoler, J Lyonnet, S Cormier-Daire, V Viskochil, D Hoffman, TL Amiel, J Chung, BHY Gordon, CT University of Washington Center for Mendelian Genomics	2020

Showing results 1 to 2 of 2