Mixed Gonadal Dysgenesis and Precocious Puberty von Iliev, D.I., Ranke, M.B., Wollmann, H.A.

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Metabolic effects of growth hormone in children von Wollmann, H.A., Ranke, M.B.

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(Epi)mutations in 11p15 significantly contribute to Silver–Russell syndrome: but are they generally involved in growth retardation? von Schönherr, N., Meyer, E., Eggermann, K., Ranke, M.B., Wollmann, H.A., Eggermann, T.

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Short Children with Low Birth Weight Born either Small for Gestational Age or Average for Gestational Age Show Similar Growth Response and Changes in Insulin-Like Growth Factor-1 t... von Ranke, M.B., Martin, D.D., Ehehalt, S., Schwarze, C.P., Serra, F., Wollmann, H.A., Schweizer, R.

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Analysis of genomic variants in the KCNQ1OT1 transcript in Silver–Russell syndrome patients von Meyer, E., Wollmann, H.A., Eggermann, T.

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LOT1 (ZAC1/PLAGL1) as Member of an Imprinted Gene Network Does Not Harbor Silver-Russell Specific Variants von Jäger, S., Schönherr, N., Spengler, S., Ranke, M.B., Wollmann, H.A., Binder, G., Eggermann, T.

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Are H19 Variants Associated with Silver-Russell Syndrome? von Schönherr, N., Binder, G., Korsch, E., Kämmerer, E., Wollmann, H.A., Eggermann, Τ.

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Significance of Basal IGF-I, IGFBP-3 and IGFBP-2 Measurements in the Diagnostics of Short Stature in Children von Ranke, M.B., Schweizer, R., Elmlinger, M.W., Weber, K., Binder, G., Schwarze, C.P., Wollmann, H.A.

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Intrauterine Wachstumsretardierung von Wollmann, H.A.

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Relevance of IGF-I, IGFBP-3, and IGFBP-2 Measurements during GH Treatment of GH-Deficient and Non-GH-Deficient Children and Adolescents von Ranke, M.B., Schweizer, R., Elmlinger, M.W., Weber, K., Binder, G., Schwarze, C.P., Wollmann, H.A.

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Experience with Growth Hormone Therapy in Turner Syndrome in a Single Centre: Low Total Height Gain, No Further Gains after Puberty Onset and Unchanged Body Proportions von Schweizer, R., Ranke, M.B., Binder, G., Herdach, F., Zapadlo, M., Grauer, M.L., Schwarze, C.P., Wollmann, H.A.

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Identification of two new polymorphisms (c2447-125A>G; c2532G>A) in the ?2-COP (COPG2) gene by screening of Silver-Russell syndrome patients von Mergenthaler, S., Blagitko-Dorfs, N., Wollmann, H.A., Ranke, M.B., Ropers, H.H., Kalscheuer, V.M., Eggermann, T.

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Identification of two new polymorphisms (c2447-125A>G; c2532G>A) in the γ2-COP (COPG2) gene by screening of Silver-Russell syndrome patients von Mergenthaler, S., Blagitko-Dorfs, N., Wollmann, H.A., Ranke, M.B., Ropers, H.H., Kalscheuer, V.M., Eggermann, T.

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Transient Pseudohypoaldosteronism with Complex Malformation of Internal Genitalia von Iliev, D.I., Petruch, U.R., Ranke, M.B., Binder, G., Leriche, C., Strotbek, G., Wollmann, H.A.

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Quantification of GRB10 in 7p12-p14 by fluorogenic 5′ nuclease chemistry and application for genetic diagnosis in Silver-Russell syndrome von Eggermann, T., Meyer, E., Wollmann, H.A.

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