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Krege, S
Walz, KH
Hauffa, BP
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Citation: S. Krege et al., Long-term follow-up of female patients with congenital adrenal hyperplasiafrom 21-hydroxylase deficiency, with special emphasis on the results of vaginoplasty, BJU INT, 86(3), 2000, pp. 253-258
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Lee, PDK
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Citation: Bp. Hauffa et al., Spontaneous growth in German children and adolescents with genetically confirmed Prader-Willi syndrome, ACT PAEDIAT, 89(11), 2000, pp. 1302-1311
Authors:
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Ranke, MB
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Citation: Mb. Ranke et al., Therapy of growth deficiency with growth hormone. Developments 10 years after the introduction of recombinant growth hormone, MONATS KIND, 148(8), 2000, pp. 746-761
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Nicolai, RD
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Citation: Rd. Nicolai et al., Serum insulin-like growth factors IGF-I and IGFBP-3 in children with slipped capital femoral epiphysis, J PED ORT B, 8(2), 1999, pp. 103-106
Authors:
Korsch, E
Peter, M
Hiort, O
Sippell, WG
Ure, BM
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Bergmann, M
Citation: E. Korsch et al., Gonadal histology with testicular carcinoma in situ in a 15-year-old 46,XYfemale patient with a premature termination is the steroidogenic acute regulatory protein causing congenital lipoid adrenal hyperplasia, J CLIN END, 84(5), 1999, pp. 1628-1632
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Haverkamp, F
Wolfle, J
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Citation: F. Haverkamp et al., Growth retardation in turner syndrome: Aneuploidy, rather than specific gene loss, may explain growth failure, J CLIN END, 84(12), 1999, pp. 4578-4582