Expanding the phenotypic spectrum of ECEL1-related congenital contracture syndromes von Shaaban, S., Duzcan, F., Yildirim, C., Chan, W.-M., Andrews, C., Akarsu, N.A., Engle, E.C.

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Congenital Fibrosis of the Extraocular Muscles Type 2, an Inherited Exotropic Strabismus Fixus, Maps to Distal 11q13 von Wang, S.M., Zwaan, J., Mullaney, P.B., Jabak, M.H., Al-Awad, A., Beggs, A.H., Engle, E.C.

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110th ENMC International Workshop: The congenital cranial dysinnervation disorders (CCDDs) von Gutowski, N.J, Bosley, T.M, Engle, E.C

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Clinical characterization of the HOXA1 syndrome BSAS variant von BOSLEY, T. M, SALIH, M. A, ALORAINY, I. A, OYSTRECK, D. T, NESTER, M, ABU-AMERO, K. K, TISCHFIELD, M. A, ENGLE, E. C

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110th ENMC International Workshop: The congenital cranial dysinnervation disorders (CCDDs): Naarden, The Netherlands, 25–27 October, 2002 von Gutowski, N.J, Bosley, T.M, Engle, E.C

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Case 27-1995: A 29-month-old girl with worsening ataxia, nystagmus, and subsequent opsoclonus and myoclonus von Engle, E.C, Hedley-Whyte, E.T

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A Japanese family with FEOM1-linked congenital fibrosis of the extraocular muscles type 1 associated with spinal canal stenosis and refinement of the FEOM1 critical region von Uyama, E., Yamada, K., Kawano, H., Chan, W.-M., Andrews, C., Yoshioka, M., Uchino, M., Engle, E.C.

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Optic nerve head and retinal abnormalities associated with congenital fibrosis of the extraocular muscles von Thomas, M.G, Maconachie, G.D.E, Kuht, H.J, Chan, W.-M, Sheth, V, Hisaund, M, McLean, R.J, Barry, B, Al-Diri, B, Proudlock, F.A, Tu, Z, Engle, E.C, Gottlob, I

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Genotypic and phenotypic spectrum of foveal hypoplasia : a multicenter study von Kuht, H.J, Maconachie, G.D.E, Han, J, Kessel, L, van Genderen, M.M, McLean, R.J, Hisaund, M, Tu, Z, Hertle, R.W, Gronskov, K, Bai, D, Wei, A, Li, W, Jiao, Y, Smirnov, V, Choi, J.-H, Tobin, M.D, Sheth, V, Purohit, R, Dawar, B, Girach, A, Strul, S, May, L, Chen, F.K, Heath Jeffery, R.C, Aamir, A, Sano, R, Jin, J, Brooks, B.P, Kohl, S, Arveiler, B, Montoliu, L, Engle, E.C, Proudlock, F.A, Nishad, G, Pani, P, Varma, G, Gottlob, I, Thomas, M.G

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(CA) repeat polymorphism in the chromosome 18 encoded dystrophin-like protein von Khurana, T.S., Engle, E.C., Bennett, R.R., Silverman, G.A., Seling, S., Bruns, G.A.P., Kunkel, L.M.

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Corrigendum to “Suppression of ϒ production in d+ Au and Au + Au collisions at s N N = 200   GeV ” [Phys. Lett. B 735 (2014) 127–137] von Adamczyk, L., Adkins, J.K., Agakishiev, G., Aggarwal, M.M., Ahammed, Z., Alekseev, I., Alford, J., Anson, C.D., Aparin, A., Arkhipkin, D., Aschenauer, E.C., Averichev, G.S., Balewski, J., Banerjee, A., Barnovska, Z., Beavis, D.R., Bellwied, R., Bhasin, A., Bhati, A.K., Bhattarai, P., Bichsel, H., Bielcik, J., Bielcikova, J., Bland, L.C., Bordyuzhin, I.G., Borowski, W., Bouchet, J., Brandin, A.V., Brovko, S.G., Bültmann, S., Bunzarov, I., Burton, T.P., Butterworth, J., Caines, H., Calderón de la Barca Sánchez, M., Cebra, D., Cendejas, R., Cervantes, M.C., Chaloupka, P., Chang, Z., Chattopadhyay, S., Chen, H.F., Chen, J.H., Chen, L., Cheng, J., Cherney, M., Chikanian, A., Christie, W., Chwastowski, J., Codrington, M.J.M., Corliss, R., Cramer, J.G., Crawford, H.J., Cui, X., Das, S., Davila Leyva, A., De Silva, L.C., Debbe, R.R., Dedovich, T.G., Deng, J., Derevschikov, A.A., Derradi de Souza, R., Dhamija, S., di Ruzza, B., Didenko, L., Dilks, C., Ding, F., Djawotho, P., Dong, X., Drachenberg, J.L., Draper, J.E., Du, C.M., Dunkelberger, L.E., Dunlop, J.C., Efimov, L.G., Engelage, J., Engle, K.S., Eppley, G., Eun, L., Evdokimov, O., Fatemi, R., Fazio, S., Fedorisin, J., Filip, P., Finch, E., Fisyak, Y., Flores, C.E., Gagliardi, C.A., Gangadharan, D.R., Garand, D., Geurts, F., Gibson, A., Girard, M., Gliske, S., Grosnick, D., Guo, Y., Gupta, A., Gupta, S., Guryn, W., Haag, B.

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