Mutations of the androgen receptor gene in patients with complete androgen insensitivity von Jakubiczka, Sibylle, Nedel, Stefanie, Werder, Edmond A., Schleiermacher, Engelbert, Theile, Ursel, Wolff, Gerhard, Wieacker, Peter

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Treatment of precocious puberty with cyproterone acetate von Werder, E A, Mürset, G, Zachmann, M, Brook, C G, Prader, A

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Excessive Thyrotropin Response to Thyrotropin-releasing Hormone in Pseudohypoparathyroidism von Werder, Edmond A, Illig, Ruth, Bernasconi, Sergio, Kind, Hanspeter, Prader, Andrea, Fischer, Jan A, Fanconi, Andreas

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TREATMENT OF PRECOCIOUS PUBERTY WITH CYPROTERONE ACETATE von WERDER, EDMOND A, MÜRSET, GERTRUD, ZACHMANN, MILO, BROOK, CHARLES G. D, PRADER, ANDEREA

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Exclusively paternal X chromosomes in a girl with short stature von SCHINZEL, A. A, ROBINSON, W. P, BINKERT, F, TORRESANI, T, WERDER, E. A

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Point mutation in the steroid-binding domain of the androgen receptor gene in a family with complete androgen insensitivity syndrome (CAIS) von JAKUBICZKA, S, WERDER, E. A, WIEACKER, P

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Exclusively paternal X chromosomes in a girl with short stature von Schinzel, Albert A, Robinson, Wendy P, Binkert, Franz, Torresani, Toni, Werder, Edmond A

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86 INCREASED PLASMA DHEA AND DHEAS AND ABSENT OR VERY LOW URINARY DHEAS, A NEW CAUSE OF HIRSUTISM (H) von Zachmann, Milo, Kempken, Bianca, Manella, Brigitte, Eiholzer, Urs, Werder, Edmond A, Otten, Albert, Prader, Andrea

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Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation von Kotzot, Dieter, Schmitt, Silke, Bernasconi, Fabiana, Robinson, Wendy P., Lurie, Iosif W., Ilyina, Helena, Méhes, Károly, Hamel, Ben C.J., Otten, Barto J., Hergersberg, Martin, Werder, Edmond, Schoenle, Eugen, Schinzel, Albert

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No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardation von Kotzot, Dieter, Lurie, Iosif W, Méhes, Károly, Werder, Edmond, Schinzel, Albert

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17α-Hydroxylase/17,20-lyase deficiency as a model to study enzymatic activity regulation : Role of phosphorylation von BIASON-LAUBER, A, KEMPKEN, B, WERDER, E, FOREST, M. G, EINAUDI, S, RANKE, M. B, MATSUO, N, BRUNELLI, V, SCHÖNLE, E. J, ZACHMANN, M

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17α-Hydroxylase/17,20-Lyase Deficiency as a Model to Study Enzymatic Activity Regulation: Role of Phosphorylation1 von Biason-Lauber, Anna, Kempken, Bianca, Werder, Edmond, Forest, Maguelone G., Einaudi, Silvia, Ranke, Michael B., Matsuo, Nobutake, Brunelli, Valeria, Schönle, Eugen J., Zachmann, Milo

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Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation von Kotzot, Dieter, Schmitt, Silke, Bernasconi, Fabiana, Robinson, Wendy P, Lurie, Iosif W, Ilyina, Helena, Méhes, Károly, Hamel, Ben C J, Otten, Barto J, Hergersberg, Martin, Werder, Edmond, Schoenle, Eugen, Schinzel, Albert

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Adrenal Function During Long-Term Anesthesia in Man 1 von Von Werder, Klaus, Stevens, Wendell C., Cromwell, Thomas H., Eger, Edmond I., Hane, Satoshi, Forsham, Peter H.

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