Utility of clinical high‐depth next generation sequencing for somatic variant detection in the PIK3CA‐related overgrowth spectrum von Hucthagowder, V., Shenoy, A., Corliss, M., Vigh‐Conrad, K.A., Storer, C., Grange, D.K., Cottrell, C.E.

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Prospective characterization of early symptom onset and progression in young pediatric patients with variants in the GLA gene across 5 years: Longitudinal data from the Fabry MOPPe... von Laney, D.A., Houde, M.F., Foley, A.L., Peck, D.S., Atherton, A.M., Manwaring, L.P., Grange, D.K., Heese, B.A., Holida, M.D., Quillin, A.L., Vinson, R., Auray-Blais, C., Hopkin, R.J.

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Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes von Shinawi, M., Coorg, R., Shimony, J.S., Grange, D.K., Al-Kateb, H.

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De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females von Palmer, E.E, Stuhlmann, T, Weinert, S, Haan, E, Van Esch, Hilde, Holvoet, M, Boyle, J, Leffler, M, Raynaud, M, Moraine, C, van Bokhoven, H, Kleefstra, T, Kahrizi, K, Najmabadi, H, Ropers, H.-H, Delgado, M.R, Sirsi, D, Golla, S, Sommer, A, Pietryga, M.P, Chung, W.K, Wynn, J, Rohena, L, Bernardo, E, Hamlin, D, Faux, B.M, Grange, D.K, Manwaring, L, Tolmie, J, Joss, S, DDD Study, Cobben, J.M, Duijkers, F.A.M, Goehringer, J.M, Challman, T.D, Hennig, F, Fischer, U, Grimme, A, Suckow, V, Musante, L, Nicholl, J, Shaw, M, Lodh, S.P, Niu, Z, Rosenfeld, J.A, Stankiewicz, P, Jentsch, T.J, Gecz, J, Field, M, Kalscheuer, V.M

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Mild fumarase deficiency and a trial of low protein diet von Kimonis, V.E., Steller, J., Sahai, I., Grange, D.K., Shoemaker, J., Zelaya, B.M., Mandell, R., Shih, K., Shih, V.

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Cantú Syndrome Is Caused by Mutations in ABCC9 von van Bon, B.W, Gilissen, C, Grange, D.K, Hennekam, R.C, Kayserili, H, Engels, H, Reutter, H, Ostergaard, J.R, Morava, Eva, Tsiakas, K, Isidor, B, Le Merrer, M, Eser, M, Wieskamp, N, de Vries, B.B, Hoischen, A

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IDH2 mutations in patients with D-2-hydroxyglutaric aciduria von Kranendijk, M, Struys, E.A, van Schaftingen, E, Gibson, K.M, Kanhai, W.A, van der Knaap, M.S, Amiel, J, Buist, N.R, Das, A.M, de Klerk, J.B, Feigenbaum, A.S, Grange, D.K, Hofstede, F.C, Holme, E, Kirk, E.P, Korrman, S.H, Morava, Eva, Morris, A, Smeitink, J, Sukhai, R.N, Vallance, H, Jakobs, C, Salomons, G.S

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TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype von Keaton, A.A., Solomon, B.D., Kauvar, E.F., El-Jaick, K.B., Gropman, A.L., Zafer, Y., Meck, J.M., Bale, S.J., Grange, D.K., Haddad, B.R., Gowans, G.C., Clegg, N.J., Delgado, M.R., Hahn, J.S., Pineda-Alvarez, D.E., Lacbawan, F., Vélez, J.I., Roessler, E., Muenke, M.

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De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability von Kury, S., Woerden, G.M. van, Besnard, T., Onori, M.P., Latypova, X., Towne, M.C., Cho, M.T., Prescott, T.E., Ploeg, M.A., Sanders, S., Stessman, H.A.F., Pujol, A., Distel, ben, Robak, L.A., Bernstein, J.A., Denomme-Pichon, A.S., Lesca, G., Sellars, E.A., Berg, J., Carre, W., Busk, O.L., Bon, B.W.M. van, Waugh, J.L., Deardorff, M., Hoganson, G.E., Bosanko, K.B., Johnson, D.S., Dabir, T., Holla, O.L., Sarkar, A., Tveten, K., Bellescize, J. de, Braathen, G.J., Terhal, P.A., Grange, D.K., Haeringen, A. van, Lam, C., Mirzaa, G., Burton, J., Bhoj, E.J., Douglas, J., Santani, A.B., Nesbitt, A.I., Helbig, K.L., Andrews, M.V., Begtrup, A., Tang, S., Gassen, K.L.I. van, Juusola, J., Foss, K., Enns, G.M., Moog, U., Hinderhofer, K., Paramasivam, N., Lincoln, S., Kusako, B.H., Lindenbaum, P., Charpentier, E., Nowak, C.B., Cherot, E., Simonet, T., Ruivenkamp, C.A.L., Hahn, S., Brownstein, C.A., Xia, F., Schmitt, S., Deb, W., Bonneau, D., Nizon, M., Quinquis, D., Chelly, J., Rudolf, G., Sanlaville, D., Parent, P., Gilbert-Dussardier, B., Toutain, A., Peart-Vissers, L.E.L.M., Boisseau, P., Vincent, M., Grabrucker, A.M., Dubourg, C., Tan, W.H., Verbeek, N.E., Granzow, M., Santen, G.W.E., Shendure, J., Isidor, B., Pasquier, L., Redon, R., Yang, Y.P., State, M.W., Kleefstra, T., Cogne, B., Petrovski, S., Retterer, K., Eichler, E.E., Agrawal, P.B., Bezieau, S., Odent, S., Elgersma, Y.

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Supplementary Material for: TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype von Keaton, A.A., Solomon, B.D., Kauvar, E.F., El-Jaick, K.B., Gropman, A.L., Zafer, Y., Meck, J.M., Bale, S.J., Grange, D.K., Haddad, B.R.

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Petrography, geochronology and source terrain characteristics of lunar meteorites Dhofar 925, 961 and Sayh al Uhaymir 449 von Joy, K.H., Nemchin, A., Grange, M., Lapen, T.J., Peslier, A.H., Ross, D.K., Zolensky, M.E., Kring, D.A.

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Protocol for the development of a multidisciplinary clinical practice guideline for the care of patients with chronic subdural haematoma von Stubbs, D.J, Davies, B.M, Dixon-Woods, M, Bashford, T.H, Braude, P, Bulters, D, Camp, S, Carr, G, Coles, J.P, Dhesi, J, Dinsmore, J, Edlmann, E, Evans, N.R, Figaji, A, Foster, E, Lecky, F, Kolias, A, Joannides, A, Moppett, I, Nathanson, M, Newcombe, V, Owen, N, Peterman, L, Proffitt, A, Skiterall, C, Whitfield, P, Wilson, S.R, Zolnourian, A, Amarouche, M, Ansari, A, Borg, N, Brennan, P.M, Brown, C, Corbett, C, Dammers, R, Das, T, Feilding, E, Galea, M, Gillespie, C, Glancz, L, Gooding, F, Grange, R, Gray, N, Hartley, P, Hassan, T, Holl, D, Jones, J, Knight, R, Luoma, V, Mee, H, Minett, T, Novak, S, Peck, G, Ralhan, S, Ramshaw, J, Richardson, D, Sadek, A.-R, Sheehan, K, Sheppard, F, Shipway, D, Singh, N, Smith, M, Sturley, R, Swart, M, Thomas, W, Uprichard, J, Yeardley, V, Menon, D.K, Hutchinson, P.J

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Protocol for the development of a multidisciplinary clinical practice guideline for the care of patients with chronic subdural haematoma von Stubbs, D.J, Davies, B.M, Dixon-Woods, M, Bashford, T.H, Braude, P, Bulters, D, Camp, S, Carr, G, Coles, J.P, Dhesi, J, Dinsmore, J, Edlmann, E, Evans, N.R, Figaji, A, Foster, E, Lecky, F, Kolias, A, Joannides, A, Moppett, I, Nathanson, M, Newcombe, V, Owen, N, Peterman, L, Proffitt, A, Skiterall, C, Whitfield, P, Wilson, S.R, Zolnourian, A, Amarouche, M, Ansari, A, Borg, N, Brennan, P.M, Brown, C, Corbett, C, Dammers, R, Das, T, Feilding, E, Galea, M, Gillespie, C, Glancz, L, Gooding, F, Grange, R, Gray, N, Hartley, P, Hassan, T, Holl, D, Jones, J, Knight, R, Luoma, V, Mee, H, Minett, T, Novak, S, Peck, G, Ralhan, S, Ramshaw, J, Richardson, D, Sadek, A.R, Sheehan, K, Sheppard, F, Shipway, D, Singh, N, Smith, M, Sturley, R, Swart, M, Thomas, W, Uprichard, J, Yeardley, V, Menon, D.K, Hutchinson, P.J

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Capless annealing of silicon implanted gallium arsenide von Grange, J.D., Wickenden, D.K.

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Contributors, May 1977 von Akello, R.J., Banerjee, D.K., Barber, P.W., Catravas, G.N., Davies, J.B., Davies, O.J., Davies, R., de Santis, P., Easter, B., Geithman, G.A., Gonda, J., Grange, J.A., Gupta, K.K., Higgins, I.D., Hoefer, W.J.R., James, D.S., Kerr, A.R., Kneppo, I., Konrad, A., Mattauch, R.J., McAulay, A.D., Milligan, T.A., Neelakantaswamy, P.S., Oliva, S.A., Olsen, R.G., Painchaud, G.R., Riblet, G.P., Riblet, H.J., Saad, S.S., Schott, F.W., Schrader, D.H., Schroeder, W.E., Stephenson, I.M., Weis, M., Yodokawa, T.

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