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La ricerca find articoli where authors phrase all words ' Magenis, RE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 35 riferimenti
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    1. Bussey, KJ; Lawce, HJ; Himoe, E; Shu, XO; Heerema, NA; Perlman, EJ; Olson, SB; Magenis, RE
      SNRPN methylation patterns in germ cell tumors as a reflection of primordial germ cell development

      GENES CHROMOSOMES & CANCER
    2. Bussey, KJ; Lawce, HJ; Himoe, E; Shu, XO; Suijkerbuijk, RF; Olson, SB; Magenis, RE
      Chromosomes 1 and 12 abnormalities in pediatric germ cell tumors by interphase fluorescence in situ hybridization

      CANCER GENETICS AND CYTOGENETICS
    3. Baty, BJ; Olson, SB; Magenis, RE; Carey, JC
      Trisomy 20 mosaicism in two unrelated girls with skin hypopigmentation andnormal intellectual development

      AMERICAN JOURNAL OF MEDICAL GENETICS
    4. Warden, CR; Pillers, DAM; Rice, MJ; Wildes, J; Livingston, JS; Clark, BA; Gilhooly, JT; Magenis, RE
      Interstitial duplication of the short arm of chromosome 1 in a newborn with congenital heart disease and multiple malformations

      AMERICAN JOURNAL OF MEDICAL GENETICS
    5. Bunzow, JR; Sonders, MS; Arttamangkul, S; Harrison, LM; Zhang, G; Quigley, DI; Darland, T; Suchland, KL; Pasumamula, S; Kennedy, JL; Olson, SB; Magenis, RE; Amara, SG; Grandy, DK
      Amphetamine, 3,4-methylenedioxymethamphetamine, lysergic acid diethylamide, and metabolites of the catecholamine neurotransmitters are agonists of a rat trace amine receptor

      MOLECULAR PHARMACOLOGY
    6. Bussey, KJ; Lawce, HJ; Olson, SB; Arthur, DC; Kalousek, DK; Krailo, M; Giller, R; Heifetz, S; Womer, R; Magenis, RE
      Chromosome abnormalities of eighty-one pediatric germ cell tumors: Sex-, age-, site-, and histopathology-related differences - A Children's Cancer Group study

      GENES CHROMOSOMES & CANCER
    7. MCMILIN KD; REISS JA; BROWN MG; BLACK MH; BUCKMASTER DA; DURUM CT; GUNTER KA; LAWCE HJ; BERRY TL; LAMB OA; OLSON CL; WEEKS FF; YOSHITOMI MJ; JACKY PB; OLSON SB; MAGENIS RE
      CLINICAL OUTCOMES OF 4 PATIENTS WITH MICRODELETION IN THE LONG ARM OFCHROMOSOME-2

      American journal of medical genetics
    8. HEINRICH MC; HOATLIN ME; ZIGLER AJ; SILVEY KV; BAKKE AC; KEEBLE WW; ZHI Y; REIFSTECK CA; GROMPE M; BROWN MG; MAGENIS RE; OLSON SB; BAGBY GC
      DNA CROSS-LINKER-INDUCED G2 M ARREST IN GROUP-C FANCONI-ANEMIA LYMPHOBLASTS REFLECTS NORMAL CHECKPOINT FUNCTION/

      Blood
    9. ELSEA SH; PURANDARE SM; ADELL RA; JUYAL RC; DAVIS JG; FINUCANE B; MAGENIS RE; PATEL PI
      DEFINITION OF THE CRITICAL INTERVAL FOR SMITH-MAGENIS-SYNDROME

      Cytogenetics and cell genetics
    10. TOTHFEJEL S; GUNTER K; MCMILIN K; REIFSTECK C; CHEN XN; KORENBERG JR; QUAN F; OLSON SB; MAGENIS RE
      HIGH-RATE OF CHROMOSOME-11 STRUCTURAL MOSAICISM IN CHROMOSOME-11 TERMINAL DELETIONS - FRAGILE SITE EXPRESSION AND CGG REPEAT EXPANSION AT FRA11B AS A GENETIC MECHANISM

      American journal of human genetics
    11. BUSSEY KJ; LAWCE HJ; OLSON SB; SHU XO; ARTHUR DC; HEIFETZ S; WOMER R; GILLER R; KRAILO M; MAGENIS RE
      LOSS OF 1P36 IN MALIGNANT PEDIATRIC GERM-CELL TUMORS

      American journal of human genetics
    12. DUONGTRAN J; PILLERS DM; RICE M; LAWCE H; MAGENIS RE
      FISHING FOR DELETION OF THE DIGEORGE CRITICAL REGION

      Journal of investigative medicine
    13. ROA BB; GREENBERG F; GUNARATNE P; SAUER CM; LUBINSKY MS; KOZMA C; MECK JM; MAGENIS RE; SHAFFER LG; LUPSKI JR
      DUPLICATION OF THE PMP22 GENE IN 17P PARTIAL TRISOMY PATIENTS WITH CHARCOT-MARIE-TOOTH TYPE-1A NEUROPATHY

      Human genetics
    14. BOUDOUSQUIE AC; LAWCE HJ; SHERMAN R; OLSON S; MAGENIS RE; CORLESS CL
      COMPLEX TRANSLOCATION(7-22) IDENTIFIED IN AN EPITHELIOID HEMANGIOENDOTHELIOMA

      Cancer genetics and cytogenetics
    15. NICKEL RE; MAGENIS RE
      NEURAL-TUBE DEFECTS AND DELETIONS OF 22Q11

      American journal of medical genetics
    16. TOTHFEJEL SE; GUNTER K; QUAN F; WOLFORD J; OLSON S; MAGENIS RE
      AN APPARENT RECOMBINANT CHROMOSOME-15 WITH CRYPTIC ISODISOMY AND PRADER-WILLI-SYNDROME

      American journal of medical genetics
    17. VISWANATHA D; KOPECKY KJ; DOSS K; RANKIN C; HEAD DR; MAGENIS RE; APPELBAUM FR; WILLMAN CL
      CORRELATION OF PML-RARA MESSENGER-RNA TRANSCRIPT TYPE WITH MORPHOLOGY, CYTOGENETICS AND CLINICAL-PARAMETERS IN ACUTE PROMYELOCYTIC LEUKEMIA

      Laboratory investigation
    18. TOTHFEJEL SE; OLSON S; GUNTER K; QUAN F; WOLFORD J; POPOVICH BW; MAGENIS RE
      THE IMPACT OF IMPRINTING - PRADER-WILLI-SYNDROME RESULTING FROM CHROMOSOME-TRANSLOCATION, RECOMBINATION, AND NONDISJUNCTION

      American journal of human genetics
    19. WHITE DM; PILLERS DAM; REISS JA; BROWN MG; MAGENIS RE
      INTERSTITIAL DELETIONS OF THE SHORT ARM OF CHROMOSOME-4 IN PATIENTS WITH A SIMILAR COMBINATION OF MULTIPLE MINOR ANOMALIES AND MENTAL-RETARDATION

      American journal of medical genetics
    20. WILLIAMS CA; ANGELMAN H; CLAYTONSMITH J; DRISCOLL DJ; HENDRICKSON JE; KNOLL JHM; MAGENIS RE; SCHINZEL A; WAGSTAFF J; WHIDDEN EM; ZORI RT
      ANGELMAN SYNDROME - CONSENSUS FOR DIAGNOSTIC-CRITERIA

      American journal of medical genetics
    21. TOTHFEJEL SE; MAGENIS RE; LEFF S; BROWN MG; COMEGYS B; LAWCE H; BERRY T; KESNER D; WEBB MJ; OLSON S
      PRENATAL-DIAGNOSIS OF CHROMOSOME-15 ABNORMALITIES IN THE PRADER-WILLIANGELMAN SYNDROME REGION BY TRADITIONAL AND MOLECULAR CYTOGENETICS/

      American journal of medical genetics
    22. SLOVAK ML; TRAWEEK ST; WILLMAN CL; HEAD DR; KOPECKY KJ; MAGENIS RE; APPELBAUM FR; FORMAN SJ
      TRISOMY-11 - AN ASSOCIATION WITH STEM PROGENITOR-CELL IMMUNOPHENOTYPE

      British Journal of Haematology
    23. ROA BB; GREENBERG F; GUNARATNE P; SAUER CM; LUBINSKY MS; KOZMA C; MECK JM; MAGENIS RE; SHAFFER LG; LUPSKI JR
      DUPLICATION OF THE PMP22 GENE IN 17P PARTIAL TRISOMY PATIENTS WITH CHARCOT-MARIE-TOOTH TYPE 1A NEUROPATHY

      American journal of human genetics
    24. MAGENIS RE; TOTHFEJEL S; OLSON S; GUNTER K
      OREGON-HEALTH-SCIENCES-UNIVERSITY STUDY - CORRELATION OF CLINICAL-DIAGNOSIS OF PRADER-WILLI AND ANGELMAN SYNDROMES AND LABORATORY TEST-RESULTS

      American journal of human genetics
    25. TOTHFEJEL S; OLSON S; DURHAM C; REISS J; MAGENIS RE
      FAMILIAL MATERNAL DELETION OF D15S113 WITH BIPARENTAL METHYLATION IMPRINT OF SNRPN IN 2 HALF-SIBLING WITH ANGELMAN-SYNDROME

      American journal of human genetics
    26. GRANDY DK; GUNTER K; HAGEN S; ZHU ZW; TOTHFEJEL S; ZHOU QY; OLSON S; MAGENIS RE
      GENOMIC ANALYSIS OF THE HUMAN KAPPA-OPIOID RECEPTOR - NO EVIDENCE FORMULTIPLE GENES

      American journal of human genetics
    27. QUAN F; ZONANA J; GUNTER K; PETERSON KL; MAGENIS RE; POPOVICH BW
      AN ATYPICAL CASE OF FRAGILE-X SYNDROME CAUSED BY A DELETION THAT INCLUDES THE FMRI GENE

      American journal of human genetics
    28. MAGENIS RE; SMITH L; NADEAU JH; JOHNSON KR; MOUNTJOY KG; CONE RD
      MAPPING OF THE ACTH, MSH, AND NEURAL (MC3 AND MC4) MELANOCORTIN RECEPTORS IN THE MOUSE AND HUMAN

      Mammalian genome
    29. NICKEL RE; PILLERS DAM; MERKENS M; MAGENIS RE; DRISCOLL DA; EMANUEL BS; ZONANA J
      VELO-CARDIO-FACIAL SYNDROME AND DIGEORGE SEQUENCE WITH MENINGOMYELOCELE AND DELETIONS OF THE 22Q11 REGION

      American journal of medical genetics
    30. SEGAL GM; MAGENIS RE; BROWN M; KEEBLE W; SMITH TD; HEINRICH MC; BAGBY GC
      REPRESSION OF FANCONI-ANEMIA GENE (FACC) EXPRESSION INHIBITS GROWTH OF HEMATOPOIETIC PROGENITOR CELLS

      The Journal of clinical investigation
    31. WOLMAN SR; SLOVAK ML; WILLMAN CL; APPELBAUM FR; MAGENIS RE
      TRISOMY 8 - A PRIMARY CYTOGENETIC ANOMALY IN LEUKEMIA

      Blood
    32. NICKEL RE; PILLERS DM; MERKENS M; MAGENIS RE; DRISCOLL DA; EMANUEL BS; ZONANA J
      VELO-CARDIO-FACIAL AND DIGEORGE SYNDROMES WITH MENINGOMYELOCELE AND DELETIONS OF THE 22Q11 REGION

      European journal of pediatric surgery
    33. OLSON S; VAHDATI M; LAWCE H; BROWN M; BUCKMASTER D; DOUGHERTY T; DURUM C; GHODSI L; SMITH L; MAGENIS RE
      INHERITED EXTRA CHROMOSOME MATERIAL ON A CHROMOSOME-9P IN A FETUS - CHARACTERIZATION WITH SPECIAL STAINS AND CHROMOSOME PAINTING

      Cytogenetics and cell genetics
    34. MAGENIS RE; BROWN MG
      COMPARATIVE EFFICACY OF MMC AND DEB-INDUCED CHROMOSOME BREAKAGE IN THE DIAGNOSIS OF FANCONI-ANEMIA

      Cytogenetics and cell genetics
    35. WARDEN CR; PILLERS DM; RICE M; WILDES J; CLARK B; MAGENIS RE
      INTERSTITIAL DUPLICATION OF THE SHORT ARM OF CHROMOSOME-1 IN A NEWBORN WITH CONGENITAL HEART-DISEASE AND MULTIPLE CONGENITAL-MALFORMATIONS

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/05/20 alle ore 03:10:37