AAAAAA

   
Results: 1-5 |
Results: 5

Authors: VANLAER L HUIZING EH VERSTREKEN M VANZUIJLEN D WAUTERS JG BOSSUYT PJ VANDEHEYNING P MCGUIRT WT SMITH RJH WILLEMS PJ LEGAN PK RICHARDSON GP VANCAMP G
Citation: L. Vanlaer et al., NONSYNDROMIC HEARING IMPAIRMENT IS ASSOCIATED WITH A MUTATION IN DFNA5, Nature genetics, 20(2), 1998, pp. 194-197

Authors: GOOSSENS FJ WAUTERS JG VANHOOF GC BOSSUYT PJ SCHATTEMAN KA LOENS K SCHARPE SL
Citation: Fj. Goossens et al., SUBREGIONAL MAPPING OF THE HUMAN LYMPHOCYTE PROLYL OLIGOPEPTIDASE GENE (PREP) TO HUMAN-CHROMOSOME 6Q22, Cytogenetics and cell genetics, 74(1-2), 1996, pp. 99-101

Authors: BOSSUYT PJ VANTIENEN MN DEGRUYTER L SMETS V DUMON J WAUTERS JG
Citation: Pj. Bossuyt et al., INCIDENCE OF LOW-FLUORESCENCE A SATELLITE REGION ON CHROMOSOME-21 ESCAPING DETECTION OF ANEUPLOIDY AT INTERPHASE BY FISH, Cytogenetics and cell genetics, 68(3-4), 1995, pp. 203-206

Authors: KOTZE MJ PEETERS AV LANGENHOVEN E WAUTERS JG VANGAAL LF
Citation: Mj. Kotze et al., PHENOTYPIC-EXPRESSION AND FREQUENCY OF FAMILIAL DEFECTIVE APOLIPOPROTEIN B-100 IN BELGIAN HYPERCHOLESTEROLEMICS, Atherosclerosis, 111(2), 1994, pp. 217-225

Authors: WAUTERS JG BOSSUYT PJ ROELEN L VANROY B DUMON J
Citation: Jg. Wauters et al., APPLICATION OF FLUORESCENCE IN-SITU HYBRIDIZATION FOR EARLY PRENATAL-DIAGNOSIS OF PARTIAL TRISOMY 6P MONOSOMY 6Q DUE TO A FAMILIAL PERICENTRIC-INVERSION/, Clinical genetics, 44(5), 1993, pp. 262-269
Risultati: 1-5 |