SIMPLE mutations in Charcot‐Marie‐Tooth disease and the potential role of its protein product in protein degradation von Saifi, Gulam Mustafa, Szigeti, Kinga, Wiszniewski, Wojciech, Shy, Michael E., Krajewski, Karen, Hausmanowa‐Petrusewicz, Irena, Kochanski, Andrzej, Reeser, Suzanne, Mancias, Pedro, Butler, Ian, Lupski, James R.

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Failure of PHA-stimulated i(12p) lymphocytes to divide in Pallister-Killian syndrome von Reeser, Suzanne L. Thornburg, Wenger, Sharon L.

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Chorionic villus sampling utilization following reports of a possible association with fetal limb defects von Cutillo, Denise M., Hammond, Elizabeth A., Reeser, Suzanne L., Kershner, Melissa A., Lukin, Barbara, Godmilow, Lynn, Donnenfeld, Alan E.

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Prenatal diagnosis of the derivative chromosome 22 associated with cat eye syndrome by fluorescence in situ hybridization von Reeser, Suzanne L., Donnenfeld, Alan E., Miller, Robert C., Sellinger, Beatrice S., Emanuel, Beverly S., Driscoll, Deborah A.

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GAD-treatment of children and adolescents with recent-onset type 1 diabetes preserves residual insulin secretion after 30 months von Ludvigsson, Johnny, Chéramy, Mikael, Axelsson, Stina, Pihl, Mikael, Åkerman, Linda, Casas, Rosaura

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