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Results: 1-18 |
Results: 18
DIFFERENTIAL EXPRESSION OF FMR1, FXR1 AND FXR2 PROTEINS IN HUMAN BRAIN AND TESTIS
Authors: TAMANINI F WILLEMSEN R VANUNEN L BONTEKOE C GALJAARD H OOSTRA BA HOOGEVEEN AT
Citation: F. Tamanini et al., DIFFERENTIAL EXPRESSION OF FMR1, FXR1 AND FXR2 PROTEINS IN HUMAN BRAIN AND TESTIS, Human molecular genetics, 6(8), 1997, pp. 1315-1322
GENE TECHNOLOGY AND SOCIAL ACCEPTANCE
Authors: GALJAARD H
Citation: H. Galjaard, GENE TECHNOLOGY AND SOCIAL ACCEPTANCE, Pathologie et biologie, 45(3), 1997, pp. 250-255
RAPID ANTIBODY-TEST FOR DIAGNOSING FRAGILE-X-SYNDROME - A VALIDATION OF THE TECHNIQUE
Authors: WILLEMSEN R SMITS A MOHKAMSING S VANBEERENDONK H DEHAAN A DEVRIES B VANDENOUWELAND A SISTERMANS E GALJAARD H OOSTRA BA
Citation: R. Willemsen et al., RAPID ANTIBODY-TEST FOR DIAGNOSING FRAGILE-X-SYNDROME - A VALIDATION OF THE TECHNIQUE, Human genetics, 99(3), 1997, pp. 308-311
RAPID ANTIBODY-TEST FOR PRENATAL-DIAGNOSIS OF FRAGILE-X-SYNDROME ON AMNIOTIC-FLUID CELLS - A NEW APPRAISAL
Authors: WILLEMSEN R LOS F MOHKAMSING S VANDENOUWELAND A DEELEN W GALJAARD H OOSTRA B
Citation: R. Willemsen et al., RAPID ANTIBODY-TEST FOR PRENATAL-DIAGNOSIS OF FRAGILE-X-SYNDROME ON AMNIOTIC-FLUID CELLS - A NEW APPRAISAL, Journal of Medical Genetics, 34(3), 1997, pp. 250-251
FMR1, FXR1 AND FXR2 PROTEINS IN HUMAN BRAIN AND TESTIS
Authors: HOOGEVEEN AT TAMANINI F WILLEMSEN R VANUNEN L BONTEKOE CJM GALJAARD H OOSTRA BA
Citation: At. Hoogeveen et al., FMR1, FXR1 AND FXR2 PROTEINS IN HUMAN BRAIN AND TESTIS, American journal of human genetics, 61(4), 1997, pp. 133-133
ACCEPTANCE OF SCREENING FOR THE FRAGILE-X-SYNDROME AMONG 1878 MENTALLY-RETARDED INDIVIDUALS IN INSTITUTIONS AND SPECIAL-SCHOOLS IN THE NETHERLANDS
Authors: DEVRIES BBA VANDENOUWELAND AMW MOHKAMSING S HALLEY DJJ TIBBEN A OOSTRA BA GALJAARD H NIERMEIJER MF
Citation: Bba. Devries et al., ACCEPTANCE OF SCREENING FOR THE FRAGILE-X-SYNDROME AMONG 1878 MENTALLY-RETARDED INDIVIDUALS IN INSTITUTIONS AND SPECIAL-SCHOOLS IN THE NETHERLANDS, American journal of medical genetics, 64(1), 1996, pp. 20-20
PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME
Authors: WILLEMSEN R OOSTERWIJK JC LOS FJ GALJAARD H OOSTRA BA
Citation: R. Willemsen et al., PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME, Lancet, 348(9032), 1996, pp. 967-968
CATHEPSIN-A DEFICIENCY IN GALACTOSIALIDOSIS - STUDIES OF PATIENTS ANDCARRIERS IN 16 FAMILIES
Authors: KLEIJER WJ GEILEN GC JANSE HC VANDIGGELEN OP ZHOU XY GALJART NJ GALJAARD H DAZZO A
Citation: Wj. Kleijer et al., CATHEPSIN-A DEFICIENCY IN GALACTOSIALIDOSIS - STUDIES OF PATIENTS ANDCARRIERS IN 16 FAMILIES, Pediatric research, 39(6), 1996, pp. 1067-1071
ASSOCIATION OF FMRP WITH RIBOSOMAL PRECURSOR PARTICLES IN THE NUCLEOLUS
Authors: WILLEMSEN R BONTEKOE C TAMANINI F GALJAARD H HOOGEVEEN A OOSTRA B
Citation: R. Willemsen et al., ASSOCIATION OF FMRP WITH RIBOSOMAL PRECURSOR PARTICLES IN THE NUCLEOLUS, Biochemical and biophysical research communications, 225(1), 1996, pp. 27-33
CHARACTERIZATION OF FMR1 PROTEINS ISOLATED FROM DIFFERENT TISSUES
Authors: VERHEIJ C DEGRAAFF E BAKKER CE WILLEMSEN R WILLEMS PJ MEIJER N GALJAARD H REUSER AJJ OOSTRA BA HOOGEVEEN AT
Citation: C. Verheij et al., CHARACTERIZATION OF FMR1 PROTEINS ISOLATED FROM DIFFERENT TISSUES, Human molecular genetics, 4(5), 1995, pp. 895-901
ELEVATED PLASMA CHITOTRIOSIDASE ACTIVITY IN VARIOUS LYSOSOMAL STORAGEDISORDERS
Authors: GUO YF HE W BOER AM WEVERS RA DEBRUIJN AM GROENER JEMM HOLLAK CEM AERTS JMFG GALJAARD H VANDIGGELEN OP
Citation: Yf. Guo et al., ELEVATED PLASMA CHITOTRIOSIDASE ACTIVITY IN VARIOUS LYSOSOMAL STORAGEDISORDERS, Journal of inherited metabolic disease, 18(6), 1995, pp. 717-722
RAPID ANTIBODY-TEST FOR FRAGILE-X SYNDROME
Authors: WILLEMSEN R MOHKAMSING S DEVRIES B DEVYS D VANDENOUWELAND A MANDEL JL GALJAARD H OOSTRA B
Citation: R. Willemsen et al., RAPID ANTIBODY-TEST FOR FRAGILE-X SYNDROME, Lancet, 345(8958), 1995, pp. 1147-1148
ACCEPTANCE OF SCREENING FOR THE FRAGILE-X SYNDROME AMONG 1878 MENTALLY-RETARDED INDIVIDUALS IN INSTITUTES AND SPECIAL SCHOOLS IN THE NETHERLANDS
Authors: DEVRIES BBA VANDENOUWELAND AMW MOHKAMSING S HALLEY DJJ TIBBEN A OOSTRA BA GALJAARD H NIERMEIJER MF
Citation: Bba. Devries et al., ACCEPTANCE OF SCREENING FOR THE FRAGILE-X SYNDROME AMONG 1878 MENTALLY-RETARDED INDIVIDUALS IN INSTITUTES AND SPECIAL SCHOOLS IN THE NETHERLANDS, American journal of human genetics, 57(4), 1995, pp. 1705-1705
INSERTION OF A T NEXT TO THE DONOR SPLICE-SITE OF INTRON-1 CAUSES ABERRANTLY SPLICED MESSENGER-RNA IN A CASE OF INFANTILE G(M1)-GANGLIOSIDOSIS
Authors: MORRONE A MORREAU H ZHOU XY ZAMMARCHI E KLEIJER WJ GALJAARD H DAZZO A
Citation: A. Morrone et al., INSERTION OF A T NEXT TO THE DONOR SPLICE-SITE OF INTRON-1 CAUSES ABERRANTLY SPLICED MESSENGER-RNA IN A CASE OF INFANTILE G(M1)-GANGLIOSIDOSIS, Human mutation, 3(2), 1994, pp. 112-120
ASSIGNMENT OF A 2ND LOCUS FOR MULTIPLE EXOSTOSES TO THE PERICENTROMERIC REGION OF CHROMOSOME-11
Authors: WU YQ HEUTINK P DEVRIES BBA SANDKUIJL LA VANDENOUWELAND AMW NIERMEIJER MF GALJAARD H REYNIERS E WILLEMS PJ HALLEY DJJ
Citation: Yq. Wu et al., ASSIGNMENT OF A 2ND LOCUS FOR MULTIPLE EXOSTOSES TO THE PERICENTROMERIC REGION OF CHROMOSOME-11, Human molecular genetics, 3(1), 1994, pp. 167-171
ROLE OF GENETICS IN HEALTH-CARE
Authors: GALJAARD H
Citation: H. Galjaard, ROLE OF GENETICS IN HEALTH-CARE, Acta paediatrica, 83, 1994, pp. 22-29
CHARACTERIZATION AND LOCALIZATION OF THE HUNTINGTON DISEASE GENE-PRODUCT
Authors: HOOGEVEEN AT WILLEMSEN R MEYER N DEROOIJ KE ROOS RAC VANOMMEN GJB GALJAARD H
Citation: At. Hoogeveen et al., CHARACTERIZATION AND LOCALIZATION OF THE HUNTINGTON DISEASE GENE-PRODUCT, Human molecular genetics, 2(12), 1993, pp. 2069-2073
CHARACTERIZATION AND LOCALIZATION OF THE FMR-1 GENE-PRODUCT ASSOCIATED WITH FRAGILE-X SYNDROME
Authors: VERHEIJ C BAKKER CE DEGRAAFF E KEULEMANS J WILLEMSEN R VERKERK AJMH GALJAARD H REUSER AJJ HOOGEVEEN AT OOSTRA BA
Citation: C. Verheij et al., CHARACTERIZATION AND LOCALIZATION OF THE FMR-1 GENE-PRODUCT ASSOCIATED WITH FRAGILE-X SYNDROME, Nature, 363(6431), 1993, pp. 722-724
Risultati: 1-18 |