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Results:
1-7
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Results: 7
Authors:
Meissner, T
Rabl, W
Mohnike, K
Scholl, S
Santer, R
Mayatepek, E
Citation: T. Meissner et al., Hyperinsulinism in syndromal disorders, ACT PAEDIAT, 90(8), 2001, pp. 856-859
Authors:
Musebeck, J
Mohnike, K
Beye, P
Tonnies, H
Neitzel, H
Schnabel, D
Gruters, A
Wieacker, PF
Stumm, M
Citation: J. Musebeck et al., Short stature homeobox-containing gene deletion screening by fluorescence in situ hybridisation in patients with short stature, EUR J PED, 160(9), 2001, pp. 561-565
Authors:
Vorwerk, P
Elsner, J
Mohnike, K
Oh, Y
Rosenfeld, RG
Mittler, U
Citation: P. Vorwerk et al., Expression of IGFBP-rP2/CTGF is specific for malignant lymphoblasts of children with acute lymphoblastic leucemia (ALL), HEMAT BLOOD, 40, 2001, pp. 85-88
Authors:
Volleth, M
Stumm, M
Mohnike, K
Kalscheuer, VM
Jakubiczka, S
Wieacker, P
Citation: M. Volleth et al., Preferential inactivation of a dupX(q23 -> q27-28) chromosome in a girl with mental retardation and dysmorphy, HUMAN HERED, 52(3), 2001, pp. 177-182
Authors:
Schmitt, HJ
Mohnike, K
Zepp, F
Herden, P
Hosbach, P
Citation: Hj. Schmitt et al., Immunogenicity and reactogenicity of the Biken acellular pertussis vaccinein young adults, VACCINE, 19(4-5), 2000, pp. 403-408
Authors:
Ranke, MB
Schwarze, CP
Mohnike, K
von Muhlendahl, KE
Keller, E
Willgerodt, H
Kiess, W
Citation: Mb. Ranke et al., Catch-up growth after childhood-onset substitution in primary hypothyroidism: Is it a guide towards optimal growth hormone treatment in idiopathic growth hormone deficiency?, HORMONE RES, 50(5), 1998, pp. 264-270
Authors:
Soyke, A
Stumm, M
Krebs, P
Kloos, DU
Wieacker, P
Elsner, J
Mohnike, K
Citation: A. Soyke et al., Familial occurrence of a del(Xp-) chromosome: Pitfall in karyotype/phenotype correlation, AM J MED G, 80(4), 1998, pp. 436-438
Risultati:
1-7
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