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La ricerca find articoli where authors phrase all words ' SMEETS D' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 30 riferimenti
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    1. Eleveld, MJ; Bodmer, D; Merkx, G; Siepman, A; Sprenger, SHE; Weterman, MAJ; Ligtenberg, MJ; Kamp, J; Stapper, W; Leuken, LWM; Smeets, D; Smits, A; van Kessel, AG
      Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15)

      GENES CHROMOSOMES & CANCER
    2. Plaja, A; Vendrell, T; Smeets, D; Sarret, E; Gili, T; Catala, V; Mediano, C; Scheres, JMJC
      Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone disease

      AMERICAN JOURNAL OF MEDICAL GENETICS
    3. Narayan, A; Tuck-Muller, C; Weissbecker, K; Smeets, D; Ehrlich, M
      Hypersensitivity to radiation-induced non-apoptotic and apoptotic death incell lines from patients with the ICF chromosome instability syndrome

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    4. Kleefstra, T; van de Zande, G; Merkx, G; Mieloo, H; Hoovers, JMN; Smeets, D
      Identification of an unbalanced cryptic translocation between the chromosomes 8 and 13 in two sisters with mild mental retardation accompanied by mild dysmorphic features

      EUROPEAN JOURNAL OF HUMAN GENETICS
    5. van Kesel, AG; Wijnhoven, H; Bodmer, D; Eleveld, M; Kiemeney, L; Mulders, P; Weterman, M; Ligtenberg, M; Smeets, D; Smits, A
      Renal cell cancer: Chromosome 3 translocations as risk

      JOURNAL OF THE NATIONAL CANCER INSTITUTE
    6. MATSUURA S; TAUCHI H; NAKAMURA A; KONDO N; SAKAMOTO S; ENDO S; SMEETS D; SOLDER B; BELOHRADSKY BH; KALOUSTIAN VMD; OSHIMURA M; ISOMURA M; NAKAMURA Y; KOMATSU K
      POSITIONAL CLONING OF THE GENE FOR NIJMEGEN BREAKAGE SYNDROME

      Nature genetics
    7. GILAD S; KHOSRAVI R; HARNIK R; ZIV Y; SHKEDY D; GALANTY Y; FRYDMAN M; LEVI J; SANAL O; CHESSA L; SMEETS D; SHILOH Y; BARSHIRA A
      IDENTIFICATION OF ATM MUTATIONS USING EXTENDED RT-PCR AND RESTRICTION-ENDONUCLEASE FINGERPRINTING, AND ELUCIDATION OF THE REPERTOIRE OF A-TMUTATIONS IN ISRAEL

      Human mutation
    8. GILAD S; KHOSRAVI R; HARNIK R; ZIV Y; SHKEDY D; GALANTY Y; FRYDMAN M; LEVI J; SANAL O; CHESSA L; SMEETS D; SHILOH Y; BARSHIRA A
      IDENTIFICATION OF ATM MUTATIONS USING EXTENDED RT-PCR AND RESTRICTION-ENDONUCLEASE FINGERPRINTING, AND ELUCIDATION OF THE REPERTOIRE OF A-TMUTATIONS IN ISRAEL

      Human mutation
    9. CARVALHAS R; CORREIA H; LANCA A; SMEETS D; CARREIRO M; CASTEDO S; CHAVES J
      INTERSTITIAL DELETION OF CHROMOSOME-21 RESULTING FROM SEGREGATION OF A PATERNAL BALANCED INTRACHROMOSOMAL INSERTION - CYTOGENETIC AND FISH ANALYSIS

      European journal of human genetics
    10. Ensinger, C; Obrist, P; Mikuz, G; Merkx, G; Smeets, D; Banziger, R; Bachmann, F; Burger, M
      Assignment of the p150 subunit of the eukaryotic initiation factor 3A gene(EIF3A) to human chromosome band 10q26 by in situ hybridisation

      CYTOGENETICS AND CELL GENETICS
    11. WIJMENGA C; VANDENHEUVEL L; STRENGMAN E; LUYTEN J; VANDERBURGT I; DEGROOT R; SMEETS D; VANDONGEN J; PEARSON P; SANDKUIJL L; WEEMAES C
      LOCALIZATION OF ICF SYNDROME BY HOMOZYGOSITY MAPPING

      Molecular immunology
    12. KOOLEN MI; VANDERMEYDEN PM; BODMER D; ELEVELD M; VANDERLOOIJ E; BRUNNER H; SMITS A; VANDENBERG E; SMEETS D; VANKESSEL AG
      A FAMILIAL CASE OF RENAL-CELL CARCINOMA AND A T(2-3) CHROMOSOME-TRANSLOCATION

      Kidney international
    13. MATSUURA K; BALMUKHANOV T; TAUCHI H; WEEMAES C; SMEETS D; CHRZANOWSKA K; ENDOU S; MATSUURA S; KOMATSU K
      RADIATION INDUCTION OF P53 IN CELLS FROM NIJMEGEN BREAKAGE SYNDROME IS DEFECTIVE BUT NOT SIMILAR TO ATAXIA-TELANGIECTASIA

      Biochemical and biophysical research communications
    14. CEROSALETTI KM; LANGE E; STRINGHAM HM; WEEMAES CMR; SMEETS D; SOLDER B; BELOHRADSKY BH; TAYLOR AMR; KARNES P; ELLIOTT A; KOMATSU K; GATTI RA; BOEHNKE M; CONCANNON P
      FINE LOCALIZATION OF THE NIJMEGEN BREAKAGE SYNDROME GENE TO 8Q21 - EVIDENCE FOR A COMMON FOUNDER HAPLOTYPE

      American journal of human genetics
    15. KROISEL PM; FRYNS JP; MATTHIJS G; BRONDUMNIELSEN K; VEJERSLEV L; VONKOSKULL H; GIRAUDON E; SAURA R; HELD K; MULLERREIBLE CR; METAXOTOU C; GENUARDI M; PIOMBO G; SCHNEIDER F; SMEETS D; VANDENOUWELAND A; PACHECO P; CORREIA H; BINKERT F; GABARRON J; GALLANO P; KRISTOFFERSSON U; ANVRET M; HOWELL R; STENHOUSE S
      QUALITY GUIDELINES AND STANDARDS FOR GENETIC LABORATORIES CLINICS IN PRENATAL-DIAGNOSIS ON FETAL SAMPLES OBTAINED BY INVASIVE PROCEDURES - AN ATTEMPT TO ESTABLISH A COMMON EUROPEAN FRAMEWORK FOR QUALITY ASSESSMENT/

      European journal of human genetics
    16. LEITE RP; SMEETS D; PORTUGAL A; SANTOS L; PINTO M
      WOLF-HIRSCHHORN SYNDROME OF PARENTAL ORIGIN IN PRENATAL-DIAGNOSIS

      Cytogenetics and cell genetics
    17. WIM JM; VUILLAUME M; CHRZANOWSKA K; SMEETS D; SPERLING K; HALL J
      NIJMEGEN BREAKAGE SYNDROME CELLS FAIL TO INDUCE THE P53-MEDIATED DNA-DAMAGE RESPONSE FOLLOWING EXPOSURE TO IONIZING-RADIATION

      Molecular and cellular biology
    18. SMEETS D; VANRAVENSWAAIJ C; DEPATER J; GERSSENSCHOORL K; VANHEMEL J; JANSSEN G; SMITS A
      AT LEAST 9 CASES OF TRISOMY 11Q23-]QTER IN ONE GENERATION AS A RESULTOF FAMILIAL T(11-13) TRANSLOCATION

      Journal of Medical Genetics
    19. MATSUURA S; WEEMAES C; SMEETS D; TAKAMI H; KONDO N; SAKAMOTO S; YANO N; NAKAMURA A; TAUCHI H; ENDO S; OSHIMURA M; KOMATSU K
      GENETIC-MAPPING USING MICROCELL-MEDIATED CHROMOSOME TRANSFER SUGGESTSA LOCUS FOR NIJMEGEN BREAKAGE SYNDROME AT CHROMOSOME 8Q21-24

      American journal of human genetics
    20. MAMMI I; ILES DE; SMEETS D; CLEMENTI M; TENCONI R
      ANESTHESIOLOGICAL PROBLEMS IN WILLIAMS-SYNDROME - THE CACNL2A LOCUS IS NOT INVOLVED

      Human genetics
    21. VANDERBURGT I; CHRZANOWSKA KH; SMEETS D; WEEMAES C
      NIJMEGEN BREAKAGE SYNDROME

      Journal of Medical Genetics
    22. GOVAERTS L; TOORMAN J; BLUPHILIPSEN MVD; SMEETS D
      ANOTHER PATIENT WITH A DELETION 14Q11.2Q13

      Annales de genetique
    23. KOMATSU K; MATSUURA S; TAUCHI H; ENDO S; KODAMA S; SMEETS D; WEEMAES C; OSHIMURA M
      THE GENE FOR NIJMEGEN BREAKAGE SYNDROME (V2) IS NOT LOCATED ON CHROMOSOME-11

      American journal of human genetics
    24. FORUS A; WEGHUIS DO; SMEETS D; FODSTAD O; MYKLEBOST O; VANKESSEL AG
      COMPARATIVE GENOMIC HYBRIDIZATION ANALYSIS OF HUMAN SARCOMAS .1. OCCURRENCE OF GENOMIC IMBALANCES AND IDENTIFICATION OF A NOVEL MAJOR AMPLICON AT 1Q21-Q22 IN SOFT-TISSUE SARCOMAS

      Genes, chromosomes & cancer
    25. FORUS A; WEGHUIS DO; SMEETS D; FODSTAD O; MYKLEBOST O; VANKESSEL AG
      COMPARATIVE GENOMIC HYBRIDIZATION ANALYSIS OF HUMAN SARCOMAS .2. IDENTIFICATION OF NOVEL AMPLICONS AT 6P AND 17P IN OSTEOSARCOMAS

      Genes, chromosomes & cancer
    26. SMITS A; MARIMAN E; VANDENHELM B; KNOERSVANSLOBBE N; SMEETS D; KREMER H; VANDERMAAREL S; HAMEL B; ROPERS HH
      NONSPECIFIC X-LINKED MENTAL-RETARDATION - IDENTIFICATION OF SEPARATE SUBTYPES BY LINKAGE STUDIES AND DETAILED CLINICAL INVESTIGATION

      Cytogenetics and cell genetics
    27. SMITS A; SMEETS D; HAMEL B; DREESEN J; DEHAAN A; VANOOST B
      PREDICTION OF MENTAL STATUS IN CARRIERS OF THE FRAGILE-X MUTATION USING CGG REPEAT LENGTH

      American journal of medical genetics
    28. WEEMAES C; SMEETS D; BAKKEREN J; VANDERBURGT I
      ICF SYNDROME

      Pediatric research
    29. JANSEN G; BARTOLOMEI M; KALSCHEUER V; MERKX G; WORMSKAMP N; MARIMAN E; SMEETS D; ROPERS HH; WIERINGA B
      NO IMPRINTING INVOLVED IN THE EXPRESSION OF DM-KINASE MESSENGER-RNAS IN MOUSE AND HUMAN TISSUES

      Human molecular genetics
    30. SMEETS D; HAMERS A; VANDERBURGT I; ELSEVIER D; VANGAAL J; MERKX G; NIEHOFF J; VAESPEETERS G; WIENEN I; WEEMAES C
      ICF SYNDROME STUDIED BY FLUORESCENCE IN-SITU HYBRIDIZATION

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 16/01/21 alle ore 11:19:22