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Results:
1-7
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Results: 7
Authors:
JAKUBICZKA S
NEDEL S
WERDER EA
SCHLEIERMACHER E
THEILE U
WOLFF G
WIEACKER P
Citation: S. Jakubiczka et al., MUTATIONS OF THE ANDROGEN RECEPTOR GENE IN PATIENTS WITH COMPLETE ANDROGEN INSENSITIVITY, Human mutation, 9(1), 1997, pp. 57-61
Authors:
SCHOENLE EJ
ZAPF J
PRADER A
TORRESANI T
WERDER EA
ZACHMANN M
Citation: Ej. Schoenle et al., REPLACEMENT OF GROWTH-HORMONE (GH) IN NORMALLY GROWING GH-DEFICIENT PATIENTS OPERATED FOR CRANIOPHARYNGIOMA, The Journal of clinical endocrinology and metabolism, 80(2), 1995, pp. 374-378
Authors:
ROBINSON WP
BINKERT F
BERNASCONI F
LORDASANCHEZ I
WERDER EA
SCHINZEL AA
Citation: Wp. Robinson et al., MOLECULAR STUDIES OF CHROMOSOMAL MOSAICISM - RELATIVE FREQUENCY OF CHROMOSOME GAIN OR LOSS AND POSSIBLE ROLE OF CELL SELECTION, American journal of human genetics, 56(2), 1995, pp. 444-451
Authors:
WERDER EA
VOUTILAINEN R
ZACHMANN M
Citation: Ea. Werder et al., VIRILIZING ADRENAL-TUMOR MIMICKING CONGENITAL ADRENAL-HYPERPLASIA WITH P450C11 (11-BETA-HYDROXYLASE) DEFICIENCY, European journal of pediatrics, 153(6), 1994, pp. 411-415
Authors:
SCHINZEL AA
ROBINSON WP
BINKERT F
TORRESANI T
WERDER EA
Citation: Aa. Schinzel et al., EXCLUSIVELY PATERNAL X-CHROMOSOMES IN A GIRL WITH SHORT STATURE, Human genetics, 92(2), 1993, pp. 175-178
Authors:
WERDER EA
TORRESANI T
NAVRATIL F
ARBENZ U
EIHOLZER U
PELET B
BURRI M
SCHWARZENBACH P
HUNZIKER U
Citation: Ea. Werder et al., PERICARDIAL-EFFUSION AS A SIGN OF ACQUIRED HYPOTHYROIDISM IN CHILDRENWITH DOWN-SYNDROME, European journal of pediatrics, 152(5), 1993, pp. 397-398
Authors:
GREGORY JW
AYNSLEYGREEN A
EVANS BAJ
HUGHES IA
WERDER EA
ZACHMANN M
Citation: Jw. Gregory et al., DEFICIENCY OF 17-KETOREDUCTASE PRESENTING BEFORE PUBERTY, Hormone research, 40(4), 1993, pp. 145-148
Risultati:
1-7
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