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YANAKIEV P
ZORN I
GRIERSON AJ
BIKKER H
DYE D
KALAYDJIEVA L
BAAS F
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Citation: H. Bikker et al., IDENTIFICATION OF 5 NOVEL INACTIVATING MUTATIONS IN THE HUMAN THYROIDPEROXIDASE GENE BY DENATURING GRADIENT GEL-ELECTROPHORESIS, Human mutation, 6(1), 1995, pp. 9-16
Authors:
BIKKER H
DENHARTOG MT
BAAS F
GONS MH
VULSMA T
DEVIJLDER JJM
Citation: H. Bikker et al., A 20-BASEPAIR DUPLICATION IN THE HUMAN THYROID PEROXIDASE GENE RESULTS IN A TOTAL IODIDE ORGANIFICATION DEFECT AND CONGENITAL HYPOTHYROIDISM, The Journal of clinical endocrinology and metabolism, 79(1), 1994, pp. 248-252
Authors:
BOLHUIS PA
PONNE NJ
BIKKER H
BAAS F
DEJONG JMBV
Citation: Pa. Bolhuis et al., MOLECULAR-BASIS OF AN ADULT FORM OF SANDHOFF DISEASE - SUBSTITUTION OF GLUTAMINE FOR ARGININE AT POSITION 505 OF THE BETA-CHAIN OF BETA-HEXOSAMINIDASE RESULTS IN A LABILE ENZYME, Biochimica et biophysica acta, 1182(2), 1993, pp. 142-146