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Results: 1-25 | 26-50 | 51-52
Results: 26-50/52
LOCALIZATION BY FLUORESCENCE IN-SITU HYBRIDIZATION OF THE HUMAN FUNCTIONAL BETA-GLUCURONIDASE GENE (GUSB) TO 7Q11.21-]Q11.22 AND 2 PSEUDOGENES TO 5P13 AND 5Q13
Authors: SPELEMAN F VERVOORT R VANROY N LIEBAERS I SLY WS LISSENS W
Citation: F. Speleman et al., LOCALIZATION BY FLUORESCENCE IN-SITU HYBRIDIZATION OF THE HUMAN FUNCTIONAL BETA-GLUCURONIDASE GENE (GUSB) TO 7Q11.21-]Q11.22 AND 2 PSEUDOGENES TO 5P13 AND 5Q13, Cytogenetics and cell genetics, 72(1), 1996, pp. 53-55
MULTIPLE POLYSOMIES IN NASAL POLYPS IN CHILDREN
Authors: SPELEMAN F DEPOTTER C VANROY N LAUREYS G
Citation: F. Speleman et al., MULTIPLE POLYSOMIES IN NASAL POLYPS IN CHILDREN, Cancer genetics and cytogenetics, 90(1), 1996, pp. 86-87
MOSAIC TETRASOMY 15Q25-]QTER IN A NEWBORN-INFANT WITH MULTIPLE ANOMALIES (VOL 63, GP 482, 1996)
Authors: VANDENENDEN A VERSCHRAEGENSPAE MR VANROY N DECALUWE W DEPRAETER C SPELEMAN F
Citation: A. Vandenenden et al., MOSAIC TETRASOMY 15Q25-]QTER IN A NEWBORN-INFANT WITH MULTIPLE ANOMALIES (VOL 63, GP 482, 1996), American journal of medical genetics, 64(3), 1996, pp. 528-528
MOSAIC TETRASOMY 15Q25-]QTER IN A NEWBORN-INFANT WITH MULTIPLE ANOMALIES
Authors: VANDENENDEN A VERSCHRAEGENSPAE MR VANROY N DECALUWE W DEPRAETER C SPELEMAN F
Citation: A. Vandenenden et al., MOSAIC TETRASOMY 15Q25-]QTER IN A NEWBORN-INFANT WITH MULTIPLE ANOMALIES, American journal of medical genetics, 63(3), 1996, pp. 482-485
BALANCED TRANSLOCATION IN A NEUROBLASTOMA PATIENT DISRUPTS A CLUSTER OF SMALL NUCLEAR-RNA UI AND TRANSFER-RNA GENES IN CHROMOSOMAL BAND 1P36
Authors: VANDERDRIFT P CHAN A LAUREYS G VANROY N SICKMANN G DENDUNNEN J WESTERVELD A SPELEMAN F VERSTEEG R
Citation: P. Vanderdrift et al., BALANCED TRANSLOCATION IN A NEUROBLASTOMA PATIENT DISRUPTS A CLUSTER OF SMALL NUCLEAR-RNA UI AND TRANSFER-RNA GENES IN CHROMOSOMAL BAND 1P36, Genes, chromosomes & cancer, 14(1), 1995, pp. 35-42
CHARACTERIZATION OF THE CHROMOSOME BREAKPOINTS IN A PATIENT WITH A CONSTITUTIONAL TRANSLOCATION T(1-17)(P36.31-P36.13-Q11.2-Q12) AND NEUROBLASTOMA
Authors: LAUREYS G VERSTEEG R SPELEMAN F VANDERDRIFT P FRANCKE U OPDENAKKER G VANROY N
Citation: G. Laureys et al., CHARACTERIZATION OF THE CHROMOSOME BREAKPOINTS IN A PATIENT WITH A CONSTITUTIONAL TRANSLOCATION T(1-17)(P36.31-P36.13-Q11.2-Q12) AND NEUROBLASTOMA, European journal of cancer, 31A(4), 1995, pp. 523-526
MOLECULAR CYTOGENETIC ANALYSIS OF 1,17 TRANSLOCATIONS IN NEUROBLASTOMA
Authors: VANROY N CHENG NC LAUREYS G OPDENAKKER G SPELEMAN F
Citation: N. Vanroy et al., MOLECULAR CYTOGENETIC ANALYSIS OF 1,17 TRANSLOCATIONS IN NEUROBLASTOMA, European journal of cancer, 31A(4), 1995, pp. 530-535
1P36 - EVERY SUBBAND A SUPPRESSOR
Authors: VERSTEEG R CARON H CHENG NC VANDERDRIFT P SLATER R WESTERVELD A VOUTE PA DELATTRE O LAUREYS G VANROY N SPELEMAN F
Citation: R. Versteeg et al., 1P36 - EVERY SUBBAND A SUPPRESSOR, European journal of cancer, 31A(4), 1995, pp. 538-541
CONSTITUTIONAL TRANSLOCATION T(1-17)(P36.31-P36.13-Q11.2Q12.1) IN A NEUROBLASTOMA PATIENT. ESTABLISHMENT OF SOMATIC-CELL HYBRIDS AND IDENTIFICATION OF PND A12M2 ON CHROMOSOME-1 AND NF1/SCYA7 ON CHROMOSOME-17 AS BREAKPOINT FLANKING SINGLE-COPY MARKERS/
Authors: LAUREYS G SPELEMAN F VERSTEEG R VANDERDRIFT P CHAN A LEROY J FRANCKE U OPDENAKKER G VANROY N
Citation: G. Laureys et al., CONSTITUTIONAL TRANSLOCATION T(1-17)(P36.31-P36.13-Q11.2Q12.1) IN A NEUROBLASTOMA PATIENT. ESTABLISHMENT OF SOMATIC-CELL HYBRIDS AND IDENTIFICATION OF PND A12M2 ON CHROMOSOME-1 AND NF1/SCYA7 ON CHROMOSOME-17 AS BREAKPOINT FLANKING SINGLE-COPY MARKERS/, Oncogene, 10(6), 1995, pp. 1087-1093
DELETION MAPPING IN NEUROBLASTOMA CELL-LINES SUGGESTS 2 DISTINCT TUMOR-SUPPRESSOR GENES IN THE 1P35-36-REGION, ONLY ONE OF WHICH IS ASSOCIATED WITH N-MYC AMPLIFICATION
Authors: CHENG NC VANROY N CHAN A BEITSMA M WESTERVELD A SPELEMAN F VERSTEEG R
Citation: Nc. Cheng et al., DELETION MAPPING IN NEUROBLASTOMA CELL-LINES SUGGESTS 2 DISTINCT TUMOR-SUPPRESSOR GENES IN THE 1P35-36-REGION, ONLY ONE OF WHICH IS ASSOCIATED WITH N-MYC AMPLIFICATION, Oncogene, 10(2), 1995, pp. 291-297
THE GENE FOR HUMAN GAP JUNCTION PROTEIN CONNEXIN37 (GJA4) MAPS TO CHROMOSOME 1P35.1, IN THE VICINITY OF D1S195
Authors: VANCAMP G COUCKE P SPELEMAN F VANROY N BEYER EC OOSTRA BA WILLEMS PJ
Citation: G. Vancamp et al., THE GENE FOR HUMAN GAP JUNCTION PROTEIN CONNEXIN37 (GJA4) MAPS TO CHROMOSOME 1P35.1, IN THE VICINITY OF D1S195, Genomics, 30(2), 1995, pp. 402-403
FULL TRIPLOIDY IN A LIVEBORN PRETERM INFANT
Authors: SMETS K SPELEMAN F VANHAESEBROUCK P VANROY N DEHOORNE J
Citation: K. Smets et al., FULL TRIPLOIDY IN A LIVEBORN PRETERM INFANT, European journal of pediatrics, 154(8), 1995, pp. 688-688
ASSIGNMENT OF THE HUMAN BETA-CATENIN GENE (CTNNB1) TO 3P22 -] P21.3 BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: VANHENGEL J NOLLET F BERX G VANROY N SPELEMAN F VANROY F
Citation: J. Vanhengel et al., ASSIGNMENT OF THE HUMAN BETA-CATENIN GENE (CTNNB1) TO 3P22 -] P21.3 BY FLUORESCENCE IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 70(1-2), 1995, pp. 68-70
IDENTIFICATION OF 2 DISTINCT CHROMOSOME-12-DERIVED AMPLIFICATION UNITS IN NEUROBLASTOMA CELL-LINE NGP
Authors: VANROY N FORUS A MYKLEBOST O CHENG NC VERSTEEG R SPELEMAN F
Citation: N. Vanroy et al., IDENTIFICATION OF 2 DISTINCT CHROMOSOME-12-DERIVED AMPLIFICATION UNITS IN NEUROBLASTOMA CELL-LINE NGP, Cancer genetics and cytogenetics, 82(2), 1995, pp. 151-154
BLEPHAROPHIMOSIS-PTOSIS-EPICANTHUS INVERSUS SYNDROME (BPES) - CLINICAL SUBTYPES AND THEIR GENOTYPE
Authors: LEROY BP MESSIAEN L VANROY N SPELEMAN F DEPAEPE A
Citation: Bp. Leroy et al., BLEPHAROPHIMOSIS-PTOSIS-EPICANTHUS INVERSUS SYNDROME (BPES) - CLINICAL SUBTYPES AND THEIR GENOTYPE, Vision research, 35, 1995, pp. 3446-3446
I-17 TRANSLOCATIONS AND OTHER CHROMOSOME-17 REARRANGEMENTS IN HUMAN PRIMARY NEUROBLASTOMA TUMORS AND CELL-LINES
Authors: VANROY N LAUREYS G CHENG NC WILLEM P OPDENAKKER G VERSTEEG R SPELEMAN F
Citation: N. Vanroy et al., I-17 TRANSLOCATIONS AND OTHER CHROMOSOME-17 REARRANGEMENTS IN HUMAN PRIMARY NEUROBLASTOMA TUMORS AND CELL-LINES, Genes, chromosomes & cancer, 10(2), 1994, pp. 103-114
A MULTIMEGABASE CLUSTER OF SNRNA AND TRANSFER-RNA GENES ON CHROMOSOME1P36 HARBORS AN ADENOVIRUS SV40 HYBRID VIRUS INTEGRATION SITE
Authors: VANDERDRIFT P CHAN A VANROY N LAUREYS G WESTERVELD A SPELEMAN F VERSTEEG R
Citation: P. Vanderdrift et al., A MULTIMEGABASE CLUSTER OF SNRNA AND TRANSFER-RNA GENES ON CHROMOSOME1P36 HARBORS AN ADENOVIRUS SV40 HYBRID VIRUS INTEGRATION SITE, Human molecular genetics, 3(12), 1994, pp. 2131-2136
THE HUMAN MCP-3 GENE (SCYA7) - CLONING, SEQUENCE-ANALYSIS, AND ASSIGNMENT TO THE C-C CHEMOKINE GENE-CLUSTER ON CHROMOSOME 17Q11.2-Q12
Authors: OPDENAKKER G FITEN P NYS G FROYEN G VANROY N SPELEMAN F LAUREYS G VANDAMME J
Citation: G. Opdenakker et al., THE HUMAN MCP-3 GENE (SCYA7) - CLONING, SEQUENCE-ANALYSIS, AND ASSIGNMENT TO THE C-C CHEMOKINE GENE-CLUSTER ON CHROMOSOME 17Q11.2-Q12, Genomics, 21(2), 1994, pp. 403-408
ABROGATION OF CLASS-I HLA EXPRESSION IN NEUROBLASTOMA ASSOCIATED WITHLONG-RANGE HYPOMETHYLATION AND LOSS OF 1P36
Authors: VERSTEEG R CHENG NC CHAN A VANROY N SPELEMAN F WESTERVELD A
Citation: R. Versteeg et al., ABROGATION OF CLASS-I HLA EXPRESSION IN NEUROBLASTOMA ASSOCIATED WITHLONG-RANGE HYPOMETHYLATION AND LOSS OF 1P36, Journal of cellular biochemistry, 1994, pp. 105-105
MULTIMEGABASE CLUSTERS OF RNA GENES ON 1P36, 1Q12-]Q21 AND 1P12
Authors: VANDERDRIFT P VANROY N WESTERVELD A SPELEMAN F VERSTEEG R
Citation: P. Vanderdrift et al., MULTIMEGABASE CLUSTERS OF RNA GENES ON 1P36, 1Q12-]Q21 AND 1P12, Cytogenetics and cell genetics, 67(3), 1994, pp. 173-173
HIGH-RESOLUTION FLUORESCENCE MAPPING OF 43 DNA MARKERS TO CHROMOSOME BAND-1P36
Authors: VANROY N VANDERDRIFT P LAUREYS G OPDENAKKER G VERSTEEG R SPELEMAN F
Citation: N. Vanroy et al., HIGH-RESOLUTION FLUORESCENCE MAPPING OF 43 DNA MARKERS TO CHROMOSOME BAND-1P36, Cytogenetics and cell genetics, 67(3), 1994, pp. 173-173
PROXIMAL DELETION OF CHROMOSOME-21 CONFIRMED BY IN-SITU HYBRIDIZATIONAND MOLECULAR STUDIES
Authors: COURTENS W PETERSEN MB NOEL JC FLAMENTDURAND J VANREGEMORTER N DELNESTE D COCHAUX P VERSCHRAEGENSPAE MR VANROY N SPELEMAN F KOENIG U VAMOS E
Citation: W. Courtens et al., PROXIMAL DELETION OF CHROMOSOME-21 CONFIRMED BY IN-SITU HYBRIDIZATIONAND MOLECULAR STUDIES, American journal of medical genetics, 51(3), 1994, pp. 260-265
DIRECT TRANSMISSION OF A TANDEM DUPLICATION IN THE SHORT ARM OF CHROMOSOME-8
Authors: DHOOGE C VANROY N CRAEN M SPELEMAN F
Citation: C. Dhooge et al., DIRECT TRANSMISSION OF A TANDEM DUPLICATION IN THE SHORT ARM OF CHROMOSOME-8, Clinical genetics, 45(1), 1994, pp. 36-39
RECURRENT 1,17 TRANSLOCATIONS IN HUMAN NEUROBLASTOMA REVEAL NONHOMOLOGOUS MITOTIC RECOMBINATION DURING THE S G2 PHASE AS A NOVEL MECHANISM FOR LOSS OF HETEROZYGOSITY/
Authors: CARON H VANSLUIS P VANROY N DEKRAKER J SPELEMAN F VOUTE PA WESTERVELD A SLATER R VERSTEEG R
Citation: H. Caron et al., RECURRENT 1,17 TRANSLOCATIONS IN HUMAN NEUROBLASTOMA REVEAL NONHOMOLOGOUS MITOTIC RECOMBINATION DURING THE S G2 PHASE AS A NOVEL MECHANISM FOR LOSS OF HETEROZYGOSITY/, American journal of human genetics, 55(2), 1994, pp. 341-347
HIGH-RESOLUTION FLUORESCENCE MAPPING OF 46 DNA MARKERS TO THE SHORT ARM OF HUMAN CHROMOSOME-1
Authors: VANROY N LAUREYS G VERSTEEG R OPDENAKKER G SPELEMAN F
Citation: N. Vanroy et al., HIGH-RESOLUTION FLUORESCENCE MAPPING OF 46 DNA MARKERS TO THE SHORT ARM OF HUMAN CHROMOSOME-1, Genomics, 18(1), 1993, pp. 71-78
Risultati: 1-25 | 26-50 | 51-52