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Results: 4

Authors: VANHAUWE P EVERETT L COUCKE P CHEN A RIS C BOLDER C OTTEN B DEVIJLDER J SMITH RJH WILLEMS PJ CREMERS CWRJ GREEN ED VANCAMP G
Citation: P. Vanhauwe et al., IDENTIFICATION OF 10 NOVEL MUTATIONS IN THE PDS GENE RESPONSIBLE FOR PENDRED-SYNDROME, European journal of human genetics, 6, 1998, pp. 205-205

Authors: VANHAUWE P EVERETT LA COUCKE P SCOTT DA KRAFT ML RISSTALPERS C BOLDER C OTTEN B DEVIJLDER JJM DIETRICH NL RAMESH A SRISAILAPATHY SCR PARVING A CREMERS CWRJ WILLEMS PJ SMITH RJH GREEN ED VANCAMP G
Citation: P. Vanhauwe et al., 2 FREQUENT MISSENSE MUTATIONS IN PENDRED-SYNDROME, Human molecular genetics (Print), 7(7), 1998, pp. 1099-1104

Authors: CREMERS CWRJ BOLDER C ADMIRAAL RJC EVERETT LA JOOSTEN FBM VANHAUWE P GREEN ED OTTEN BJ
Citation: Cwrj. Cremers et al., PROGRESSIVE SENSORINEURAL HEARING-LOSS AND A WIDENED VESTIBULAR AQUEDUCT IN PENDRED-SYNDROME, Archives of otolaryngology, head & neck surgery, 124(5), 1998, pp. 501-505

Authors: CREMERS CWRJ ADMIRAAL RJC HUYGEN PLM BOLDER C EVERETT LA JOOSTEN FBM GREEN ED VANCAMP G OTTEN BJ
Citation: Cwrj. Cremers et al., PROGRESSIVE HEARING-LOSS, HYPOPLASIA OF THE COCHLEA AND WIDENED VESTIBULAR AQUEDUCTS ARE VERY COMMON FEATURES IN PENDREDS-SYNDROME, International journal of pediatric otorhinolaryngology, 45(2), 1998, pp. 113-123
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