Showing 1 - 2 results of 2 for search 'Medne, L', query time: 0.02s
Refine Results
-
1
Subtelomeric deletions of chromosome 9q: a novel microdeletion syndrome. by Stewart, DR, Huang, A, Faravelli, F, Anderlid, B, Medne, L, Ciprero, K, Kaur, M, Rossi, E, Tenconi, R, Nordenskjöld, M, Gripp, K, Nicholson, L, Meschino, W, Capua, E, Quarrell, O, Flint, J, Irons, M, Giampietro, P, Schowalter, D, Zaleski, C, Malacarne, M, Zackai, E, Spinner, N, Krantz, I
Published 2004Journal article -
2
STAC3 variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility. by Zaharieva, IT, Sarkozy, A, Munot, P, Manzur, A, O'Grady, G, Rendu, J, Malfatti, E, Amthor, H, Prof Laurent Servais, Urtizberea, JA, Neto, OA, Zanoteli, E, Donkervoort, S, Taylor, J, Dixon, J, Poke, G, Foley, AR, Holmes, C, Williams, G, Holder, M, Yum, S, Medne, L, Quijano-Roy, S, Romero, NB, Fauré, J, Feng, L, Bastaki, L, Davis, MR, Phadke, R, Sewry, CA, Bönnemann, CG, Jungbluth, H, Bachmann, C, Treves, S, Muntoni, F
Published 2018Journal article