MLL2 mutation spectrum in 45 patients with Kabuki syndrome von Paulussen, Aimée D.C, Stegmann, Alexander P.A, Blok, Marinus J, Tserpelis, Demis, Posma-Velter, Crool, Detisch, Yvonne, Smeets, Eric E.J.G.L, Wagemans, Annemieke, Schrander, Jaap J.P, van den Boogaard, Marie-José H, van der Smagt, Jasper, van Haeringen, Arie, Stolte-Dijkstra, Irene, Kerstjens-Frederikse, Wilhelmina S, Mancini, Grazia M, Wessels, Marja W, Hennekam, Raoul C.M, Vreeburg, Maaike, Geraedts, Joep, de Ravel, Thomy, Fryns, Jean-Pierre, Smeets, Hubert J, Devriendt, Koenraad, Schrander-Stumpel, Constance T.R.M

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Prader-Willi syndrome: Causes of death in an international series of 27 cases von Schrander-Stumpel, Constance Th.R.M., Curfs, Leopold M.G., Sastrowijoto, Prapto, Cassidy, Suzanne B., Schrander, Jaap J.P., Fryns, Jean-Pierre

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Kabuki syndrome: Clinical data in 20 patients, literature review, and further guidelines for preventive management von Schrander-Stumpel, Constance Th.R.M., Spruyt, Liesbeth, Curfs, Leopold M.G., Defloor, Truus, Schrander, Jaap J.P.

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MLL2 mutation spectrum in 45 patients with Kabuki syndrome von Paulussen, Aimée D.C, Stegmann, Alexander P.A, Blok, Marinus J, Tserpelis, Demis, Posma-Velter, Crool, Detisch, Yvonne, Smeets, Eric E.J.G.L, Wagemans, Annemieke, Schrander, Jaap J.P, van den Boogaard, Marie-José H, van der Smagt, Jasper, van Haeringen, Arie, Stolte-Dijkstra, Irene, Kerstjens-Frederikse, Wilhelmina S, Mancini, Grazia M, Wessels, Marja W, Hennekam, Raoul C.M, Vreeburg, Maaike, Geraedts, Joep, de Ravel de l'Argentière, Thomy, Fryns, Jean-Pierre, Smeets, Hubert J, Devriendt, Koenraad, Schrander-Stumpel, Constance T.R.M

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SOY AND PROTEINHYDROLYSATE INTOLERANCE IN INFANTS WITH COW'S MILKPROTEIN INTOLERANCE. 743 von Schrander, Jaap J.P, Forget, Philippe P, Nord, Asa

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51CR-EDTA INTESTINAL PERMEABILITY AND MILK RAST IN CHILDREN WITH COW'S MILK PROTEIN INTOLERANCE (CMPI). 65 von Schrander, Jaap J.P, Marcelis, Carlo L.M, Forget, Philippe P, Kester, Arnold

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Auditory canal atresia, humeroscapular synostosis, and other skeletal abnormalities: Confirmation of the autosomal recessive “SAMS” syndrome von ter Heide, Henriette, Bulstra, Sjoerd K., Reekers, Ad, Schrander, Jaap J.P., Schrander‐Stumpel, Constance T.R.M.

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Auditory canal atresia, humeroscapular synostosis, and other skeletal abnormalities: Confirmation of the autosomal recessive "SAMS" syndrome von ter Heide, Henriette, Bulstra, Sjoerd K., Reekers, Ad, Schrander, Jaap J.P., Schrander-Stumpel, Constance T.R.M.

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