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Results: 1-7 |
Results: 7

Authors: KOZAK L FRANCOVA H PIJACKOVA A SENY JU STASTNA S SPICKOVA K BZDUCH V
Citation: L. Kozak et al., MUTATIONS IN THE GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE GENE IN CZECH AND SLOVAK GALACTOSEMIC PATIENTS, European journal of human genetics, 6, 1998, pp. 4094-4094

Authors: BZDUCH V
Citation: V. Bzduch, WILLIAMS-SYNDROME IN SLOVAKIA, American journal of medical genetics, 65(4), 1996, pp. 366-366

Authors: BZDUCH V
Citation: V. Bzduch, NOONAN AND WILLIAMS SYNDROMES - BASIC DIFFERENTIAL-DIAGNOSIS, Clinical pediatrics, 34(11), 1995, pp. 622-623

Authors: BZDUCH V
Citation: V. Bzduch, RADIOULNAR SYNOSTOSIS IN WILLIAMS-SYNDROME - A HISTORICAL OVERVIEW, American journal of medical genetics, 50(4), 1994, pp. 386-386

Authors: BZDUCH V MASURA J
Citation: V. Bzduch et J. Masura, IMPORTANCE OF USING 2-DIMENSIONAL ECHOCARDIOGRAPHY IN FAMILIAL SUPRAVALVULAR AORTIC-STENOSIS, American journal of medical genetics, 49(4), 1994, pp. 454-454

Authors: GLOS J BZDUCH V LISY L JARIABKOVA K
Citation: J. Glos et al., LARGE MIRROR MOVEMENTS OF UPPER EXTREMITIES IN WILLIAMS-SYNDROME, Pediatric neurology, 9(5), 1993, pp. 414-414

Authors: BZDUCH V
Citation: V. Bzduch, HYPERCALCEMIC PHASE OF WILLIAMS-SYNDROME, The Journal of pediatrics, 123(3), 1993, pp. 496-496
Risultati: 1-7 |