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Results: 1-25 | 26-48
Results: 1-25/48
CYTOGENETIC AND MOLECULAR ANALYSIS OF A T(1-22)(P36-Q11.2) IN A RHABDOID TUMOR WITH A PUTATIVE HOMOZYGOUS DELETION OF CHROMOSOME-22
Authors: ROSTY C PETER M ZUCMAN J VALIDIRE P DELATTRE O AURIAS A
Citation: C. Rosty et al., CYTOGENETIC AND MOLECULAR ANALYSIS OF A T(1-22)(P36-Q11.2) IN A RHABDOID TUMOR WITH A PUTATIVE HOMOZYGOUS DELETION OF CHROMOSOME-22, Genes, chromosomes & cancer, 21(2), 1998, pp. 82-89
HSNF5 INI1, A NEW TUMOR-SUPPRESSOR INVOLVED IN THE REMODELING OF CHROMATIN STRUCTURE/
Authors: DELATTRE O VERSTEEGE I SEVENET N LANGE J AURIAS A
Citation: O. Delattre et al., HSNF5 INI1, A NEW TUMOR-SUPPRESSOR INVOLVED IN THE REMODELING OF CHROMATIN STRUCTURE/, MS. Medecine sciences, 14(10), 1998, pp. 1122-1123
TRUNCATING MUTATIONS OF HSNF5 INI1 IN AGGRESSIVE PEDIATRIC CANCER/
Authors: VERSTEEGE I SEVENET N LANGE J ROUSSEAUMERCK MF AMBROS P HANDGRETINGER R AURIAS A DELATTRE O
Citation: I. Versteege et al., TRUNCATING MUTATIONS OF HSNF5 INI1 IN AGGRESSIVE PEDIATRIC CANCER/, Nature, 394(6689), 1998, pp. 203-206
COMPARISON OF COMPARATIVE GENOMIC HYBRIDIZATION WITH CONVENTIONAL KARYOTYPE AND CLASSICAL FLUORESCENCE IN-SITU HYBRIDIZATION FOR PRENATAL AND POSTNATAL DIAGNOSIS OF UNBALANCED CHROMOSOME-ABNORMALITIES
Authors: LAPIERRE JM CACHEUX V COLLOT N DASILVA F HERVY N RIVET D ROMANA S WISS A BENZAKEN B AURIAS A TACHDJIAN G
Citation: Jm. Lapierre et al., COMPARISON OF COMPARATIVE GENOMIC HYBRIDIZATION WITH CONVENTIONAL KARYOTYPE AND CLASSICAL FLUORESCENCE IN-SITU HYBRIDIZATION FOR PRENATAL AND POSTNATAL DIAGNOSIS OF UNBALANCED CHROMOSOME-ABNORMALITIES, Annales de genetique, 41(3), 1998, pp. 133-140
MOLECULAR CYTOGENETIC CHARACTERIZATION OF THE CATCH-22 REGION DISRUPTED BY A DE-NOVO UNBALANCED TRANSLOCATION
Authors: CANKIKLAIN N DEBEVEC M BESLIC N AURIAS A MAIRAL A
Citation: N. Cankiklain et al., MOLECULAR CYTOGENETIC CHARACTERIZATION OF THE CATCH-22 REGION DISRUPTED BY A DE-NOVO UNBALANCED TRANSLOCATION, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 204-204
MOLECULAR CYTOGENETIC STUDIES ON RHABDOID TUMORS
Authors: ROUSSEAUMERCK MF ROSTY C HEIMAN P AURIAS A
Citation: Mf. Rousseaumerck et al., MOLECULAR CYTOGENETIC STUDIES ON RHABDOID TUMORS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 379-379
MULTIPLE CHROMOSOMAL MECHANISMS GENERATE AN EWS FLI1 OR AN EWS/ERG FUSION GENE IN EWING TUMORS/
Authors: DESMAZE C BRIZARD F TURCCAREL C MELOT T DELATTRE O THOMAS G AURIAS A
Citation: C. Desmaze et al., MULTIPLE CHROMOSOMAL MECHANISMS GENERATE AN EWS FLI1 OR AN EWS/ERG FUSION GENE IN EWING TUMORS/, Cancer genetics and cytogenetics, 97(1), 1997, pp. 12-19
SPECTRUM OF CLINICAL-FEATURES ASSOCIATED WITH INTERSTITIAL CHROMOSOME22Q11 DELETIONS - A EUROPEAN COLLABORATIVE STUDY
Authors: RYAN AK GOODSHIP JA WILSON DI PHILIP N LEVY A SEIDEL H SCHUFFENHAUER S OECHSLER H BELOHRADSKY B PRIEUR M AURIAS A RAYMOND FL CLAYTONSMITH J HATCHWELL E MCKEOWN C BEEMER FA DALLAPICCOLA B NOVELLI G HURST JA IGNATIUS J GREEN AJ WINTER RM BRUETON L BRONDUMNIELSEN K STEWART F VANESSEN T PATTON M PATERSON J SCAMBLER PJ
Citation: Ak. Ryan et al., SPECTRUM OF CLINICAL-FEATURES ASSOCIATED WITH INTERSTITIAL CHROMOSOME22Q11 DELETIONS - A EUROPEAN COLLABORATIVE STUDY, Journal of Medical Genetics, 34(10), 1997, pp. 798-804
ESTABLISHMENT OF A TRANSCRIPTION MAP IN THE 22Q11.2 MICRODELETION SYNDROME CRITICAL REGION
Authors: DEMCZUK S AURIAS A EYDOUX P
Citation: S. Demczuk et al., ESTABLISHMENT OF A TRANSCRIPTION MAP IN THE 22Q11.2 MICRODELETION SYNDROME CRITICAL REGION, American journal of human genetics, 61(4), 1997, pp. 1355-1355
STRUCTURAL ORGANIZATION OF THE WD REPEAT PROTEIN-ENCODING GENE HIRA IN THE DIGEORGE-SYNDROME CRITICAL REGION OF HUMAN-CHROMOSOME-22
Authors: LORAIN S DEMCZUK S LAMOUR V TOTH S AURIAS A ROE BA LIPINSKI M
Citation: S. Lorain et al., STRUCTURAL ORGANIZATION OF THE WD REPEAT PROTEIN-ENCODING GENE HIRA IN THE DIGEORGE-SYNDROME CRITICAL REGION OF HUMAN-CHROMOSOME-22, PCR methods and applications, 6(1), 1996, pp. 43-50
ISOLATION OF A NOVEL GENE FROM THE DIGEORGE-SYNDROME CRITICAL REGION WITH HOMOLOGY TO DROSOPHILA GDL AND TO HUMAN LAMC1 GENES
Authors: DEMCZUK S THOMAS G AURIAS A
Citation: S. Demczuk et al., ISOLATION OF A NOVEL GENE FROM THE DIGEORGE-SYNDROME CRITICAL REGION WITH HOMOLOGY TO DROSOPHILA GDL AND TO HUMAN LAMC1 GENES, Human molecular genetics, 5(5), 1996, pp. 633-638
FAMILIAL NON-SYNDROMIC CONOTRUNCAL DEFECTS ARE NOT ASSOCIATED WITH A 22Q11 MICRODELETION
Authors: DEBRUS S BERGER G DEMEEUS A SAUER U GUILLAUMONT S VOISIN M BOZIO A DEMCZUK S AURIAS A BOUVAGNET P
Citation: S. Debrus et al., FAMILIAL NON-SYNDROMIC CONOTRUNCAL DEFECTS ARE NOT ASSOCIATED WITH A 22Q11 MICRODELETION, Human genetics, 97(2), 1996, pp. 138-144
AN EWS ERG FUSION WITH A TRUNCATED N-TERMINAL DOMAIN OF EWS IN A EWINGS TUMOR/
Authors: PETER M MUGNERET F AURIAS A THOMAS G MAGDELENAT H DELATTRE O
Citation: M. Peter et al., AN EWS ERG FUSION WITH A TRUNCATED N-TERMINAL DOMAIN OF EWS IN A EWINGS TUMOR/, International journal of cancer, 67(3), 1996, pp. 339-342
LOCALIZATION OF TEC TO 9Q22.3-Q31 BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: KLEINFINGER P LABELLE Y MELOT T THOMAS G DELATTRE O AURIAS A
Citation: P. Kleinfinger et al., LOCALIZATION OF TEC TO 9Q22.3-Q31 BY FLUORESCENCE IN-SITU HYBRIDIZATION, Annales de genetique, 39(4), 1996, pp. 233-235
INTEREST OF THE DIRVISH TECHNIQUE IN THE SCREENING FOR MICRODELETIONS
Authors: MAAREK O THOMAS G AURIAS A
Citation: O. Maarek et al., INTEREST OF THE DIRVISH TECHNIQUE IN THE SCREENING FOR MICRODELETIONS, Annales de genetique, 39(3), 1996, pp. 173-175
SCREENING FOR GERM-LINE MUTATIONS IN THE NF2 GENE
Authors: MEREL P HOANGXUAN K SANSON M BIJLSMA E ROULEAU G LAURENTPUIG P PULST S BASER M LENOIR G STERKERS JM PHILIPPON JL RESCHE F MAUTNER VF FISCHER G HULSEBOS T AURIAS A DELATTRE O THOMAS G
Citation: P. Merel et al., SCREENING FOR GERM-LINE MUTATIONS IN THE NF2 GENE, Genes, chromosomes & cancer, 12(2), 1995, pp. 117-127
A HUMAN HOMOLOG OF THE SACCHAROMYCES-CEREVISIAE HIR1 AND HIR2 TRANSCRIPTIONAL REPRESSORS CLONED FROM THE DIGEORGE-SYNDROME CRITICAL REGION
Authors: LAMOUR V LECLUSE Y DESMAZE C SPECTOR M BODESCOT M AURIAS A OSLEY MA LIPINSKI M
Citation: V. Lamour et al., A HUMAN HOMOLOG OF THE SACCHAROMYCES-CEREVISIAE HIR1 AND HIR2 TRANSCRIPTIONAL REPRESSORS CLONED FROM THE DIGEORGE-SYNDROME CRITICAL REGION, Human molecular genetics, 4(5), 1995, pp. 791-799
CLONING OF A BALANCED TRANSLOCATION BREAKPOINT IN THE DIGEORGE-SYNDROME CRITICAL REGION AND ISOLATION OF A NOVEL POTENTIAL ADHESION RECEPTOR GENE IN ITS VICINITY
Authors: DEMCZUK S ALEDO R ZUCMAN J DELATTRE O DESMAZE C DAUPHINOT L JALBERT P ROULEAU GA THOMAS G AURIAS A
Citation: S. Demczuk et al., CLONING OF A BALANCED TRANSLOCATION BREAKPOINT IN THE DIGEORGE-SYNDROME CRITICAL REGION AND ISOLATION OF A NOVEL POTENTIAL ADHESION RECEPTOR GENE IN ITS VICINITY, Human molecular genetics, 4(4), 1995, pp. 551-558
ONCOGENIC CONVERSION OF A NOVEL ORPHAN NUCLEAR RECEPTOR BY CHROMOSOME-TRANSLOCATION
Authors: LABELLE Y ZUCMAN J STENMAN G KINDBLOM LG KNIGHT J TURCCAREL C DOCKHORNDWORNICZAK B MANDAHL N DESMAZE C PETER M AURIAS A DELATTRE O THOMAS G
Citation: Y. Labelle et al., ONCOGENIC CONVERSION OF A NOVEL ORPHAN NUCLEAR RECEPTOR BY CHROMOSOME-TRANSLOCATION, Human molecular genetics, 4(12), 1995, pp. 2219-2226
INTERSTITIAL 22Q11 MICRODELETION EXCLUDING THE ADU BREAKPOINT IN A PATIENT WITH DIGEORGE-SYNDROME
Authors: LEVY A DEMCZUK S AURIAS A DEPETRIS D MATTEI MG PHILIP N
Citation: A. Levy et al., INTERSTITIAL 22Q11 MICRODELETION EXCLUDING THE ADU BREAKPOINT IN A PATIENT WITH DIGEORGE-SYNDROME, Human molecular genetics, 4(12), 1995, pp. 2417-2419
PHYSICAL MAPPING OF 30 CA REPEATS ON HUMAN-CHROMOSOME-22
Authors: DEMCZUK S DELATTRE O VIGNAL A WEISSENBACH J THOMAS G AURIAS A
Citation: S. Demczuk et al., PHYSICAL MAPPING OF 30 CA REPEATS ON HUMAN-CHROMOSOME-22, Genomics, 27(2), 1995, pp. 345-347
EXCESS OF DELETIONS OF MATERNAL ORIGIN IN THE DIGEORGE VELO-CARDIO-FACIAL SYNDROMES - A STUDY OF 22 NEW PATIENTS AND REVIEW OF THE LITERATURE/
Authors: DEMCZUK S LEVY A AUBRY M CROQUETTE MF PHILIP N PRIEUR M SAUER U BOUVAGNET P ROULEAU GA THOMAS G AURIAS A
Citation: S. Demczuk et al., EXCESS OF DELETIONS OF MATERNAL ORIGIN IN THE DIGEORGE VELO-CARDIO-FACIAL SYNDROMES - A STUDY OF 22 NEW PATIENTS AND REVIEW OF THE LITERATURE/, Human genetics, 96(1), 1995, pp. 9-13
IN-SITU HYBRIDIZATION OF FLUORESCENT-PROBES ON CHROMOSOMES, NUCLEI ORSTRETCHED DNA - APPLICATIONS IN PHYSICAL MAPPING AND CHARACTERIZATIONOF GENOMIC REARRANGEMENTS
Authors: DESMAZE C AURIAS A
Citation: C. Desmaze et A. Aurias, IN-SITU HYBRIDIZATION OF FLUORESCENT-PROBES ON CHROMOSOMES, NUCLEI ORSTRETCHED DNA - APPLICATIONS IN PHYSICAL MAPPING AND CHARACTERIZATIONOF GENOMIC REARRANGEMENTS, Cellular and molecular biology, 41(7), 1995, pp. 925-931
DIGEORGE-SYNDROME AND RELATED SYNDROMES ASSOCIATED WITH 22Q11.2 DELETIONS - A REVIEW
Authors: DEMCZUK S AURIAS A
Citation: S. Demczuk et A. Aurias, DIGEORGE-SYNDROME AND RELATED SYNDROMES ASSOCIATED WITH 22Q11.2 DELETIONS - A REVIEW, Annales de genetique, 38(2), 1995, pp. 59-76
NEUROFIBROMATOSIS TYPE-2
Authors: THOMAS G MEREL P SANSON M HOANGXUAN K ZUCMAN J DESMAZE C MELOT T AURIAS A DELATTRE O
Citation: G. Thomas et al., NEUROFIBROMATOSIS TYPE-2, European journal of cancer, 30A(13), 1994, pp. 1981-1987
Risultati: 1-25 | 26-48