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La ricerca find articoli where authors phrase all words ' Chong, SS' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 29 riferimenti
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    1. Mertens, C; Hofmann, I; Wang, ZX; Teichmann, M; Chong, SS; Schnolzer, M; Franke, WW
      Nuclear particles containing RNA polymerase III complexes associated with the junctional plaque protein plakophilin 2

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    2. Chong, SS; Hu, P; Hernandez, N
      Reconstitution of transcription from the human U6 small nuclear RNA promoter with eight recombinant polypeptides and a partially purified RNA polymerase III complex

      JOURNAL OF BIOLOGICAL CHEMISTRY
    3. Tan, ASC; Quah, TC; Low, PS; Chong, SS
      A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for alpha-thalassemia

      BLOOD
    4. Chong, SS; Boehm, CD; Cutting, GR; Higgs, DR
      Simplified multiplex-PCR diagnosis of common southeast Asian deletional determinants of alpha-thalassemia

      CLINICAL CHEMISTRY
    5. Chong, SS; Boehm, CD; Higgs, DR; Cutting, GR
      Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia

      BLOOD
    6. Boehm, CD; Cutting, GR; Lachtermacher, MB; Moser, HW; Chong, SS
      Accurate DNA-based diagnostic and carrier testing for X-linked adrenoleukodystrophy

      MOLECULAR GENETICS AND METABOLISM
    7. Higgs, DR; Ayyub, H; Chong, SS
      The --(THAI) and --(FIL) determinants of alpha thalassemia in Taiwan

      AMERICAN JOURNAL OF HEMATOLOGY
    8. Kozma, C; Chong, SS; Meck, JM
      Interstitial deletion of 4p15.32p16.3 in a boy with minor anomalies, hearing loss, borderline intelligence, and oligodontia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    9. CHONG SS; YU XH; MAN ZH
      ROBUST ADAPTIVE SLIDING MODE CONTROL WITH MODIFIED REGRESSOR MATRIX AND COMPOSITE ADAPTATION FOR ROBOTIC MANIPULATORS

      Advanced robotics
    10. HIROTSUNE S; PACK SD; CHONG SS; ROBBINS CM; PAVAN WJ; LEDBETTER DH; WYNSHAWBORIS A
      GENOMIC ORGANIZATION OF THE MURINE MILLER-DIEKER LISSENCEPHALY REGION- CONSERVATION OF LINKAGE WITH THE HUMAN REGION/

      PCR methods and applications
    11. CHONG SS; PACK SD; ROSCHKE AV; TANIGAMI A; CARROZZO R; SMITH ACM; DOBYNS WB; LEDBETTER DH
      A REVISION OF THE LISSENCEPHALY AND MILLER-DIEKER SYNDROME CRITICAL REGIONS IN CHROMOSOME 17P13.3

      Human molecular genetics
    12. LONIGRO C; CHONG SS; SMITH ACM; DOBYNS WB; CARROZZO R; LEDBETTER DH
      POINT MUTATIONS AND AN INTRAGENIC DELETION IN LIS1, THE LISSENCEPHALYCAUSATIVE GENE IN ISOLATED LISSENCEPHALY SEQUENCE AND MILLER-DIEKER SYNDROME

      Human molecular genetics
    13. CHONG SS; ALMQVIST E; TELENIUS H; LATRAY L; NICHOL K; BOURDELATPARKS B; GOLDBERG YP; HADDAD BR; RICHARDS F; SILLENCE D; GREENBERG CR; IVES E; VANDENENGH G; HUGHES MR; HAYDEN MR
      CONTRIBUTION OF DNA-SEQUENCE AND CAG SIZE TO MUTATION FREQUENCIES OF INTERMEDIATE ALLELES FOR HUNTINGTON DISEASE - EVIDENCE FROM SINGLE SPERM ANALYSES

      Human molecular genetics
    14. ALMQVIST E; CHONG SS; NICHOL K; TELENIUS H; LATRAY L; BOURDELATPARKS B; HADDAD BR; SQUITIERI F; ANVRET M; VANDENENGH G; HAYDEN M
      DIFFERENT MUTATION-RATES OF SIMILAR SIZED CAG TRACTS OF AFFECTED HUNTINGTON-DISEASE CHROMOSOMES BY SINGLE SPERM ANALYSIS

      American journal of human genetics
    15. CHONG SS; TANIGAMI A; ROSCHKE AV; LEDBETTER DH
      14-3-3-EPSILON HAS NO HOMOLOGY TO LIS1 AND LIES TELOMERIC TO IT ON CHROMOSOME 17P13.3 OUTSIDE THE MILLER-DIEKER SYNDROME CHROMOSOME REGION

      PCR methods and applications
    16. CHONG SS; MCCALL AE; COTA J; SUBRAMONY SH; ORR HT; HUGHES MR; ZOGHBI HY
      GAMETIC AND SOMATIC TISSUE-SPECIFIC HETEROGENEITY OF THE EXPANDED SCA1 CAG REPEAT IN SPINOCEREBELLAR ATAXIA TYPE-1

      Nature genetics
    17. CHONG SS; KOZAK CA; LIU LT; KRISTJANSSON K; DUNN ST; BOURDEAU JE; HUGHES MR
      CLONING, GENETIC-MAPPING, AND EXPRESSION ANALYSIS OF A MOUSE RENAL SODIUM-DEPENDENT PHOSPHATE COTRANSPORTER

      American journal of physiology. Renal, fluid and electrolyte physiology
    18. VANDENVEYVER IB; CHONG SS; COTA J; BENNETT PR; FISK NM; HANDYSIDE AH; CARTRON JP; LEVANKIM C; COLIN Y; SNABES MC; MOISE KJ; HUGHES MR
      SINGLE-CELL ANALYSIS OF THE RHD BLOOD-TYPE FOR USE IN PREIMPLANTATIONDIAGNOSIS IN THE PREVENTION OF SEVERE HEMOLYTIC-DISEASE OF THE NEWBORN

      American journal of obstetrics and gynecology
    19. HUGHES MR; HADDAD BR; SUBRAMANIAN S; NASONKIN I; COTA J; CHONG SS
      SINGLE-CELL DETECTION OF THE FMR1, HD, AND SCA1 TRINUCLEOTIDE REPEATS- APPLICATION TO PREIMPLANTATION DIAGNOSIS AND INSTABILITY ANALYSIS OF FRAGILE-X SYNDROME, HUNTINGTON DISEASE, AND SPINO-CEREBELLAR ATAXIA TYPE-1

      American journal of human genetics
    20. HADDAD BR; CHONG SS; SUBRAMANIAN S; COTA J; HUGHES MR
      GENETIC TYPING OF SINGLE CELLS USING MULTIPLE TETRAMERIC TANDEM REPEATS AFTER WHOLE GENOME AMPLIFICATION

      American journal of human genetics
    21. CHONG SS; PACK S; TANIGAMI A; CARROZZO R; DOBYNS WB; LEDBETTER DH
      SYSTEMATIC DELETION ANALYSIS OF MDS AND ILS PATIENTS EXCLUDES A CANDIDATE GENE AND DELINEATES THE LISSENCEPHALY GENE LOCUS

      American journal of human genetics
    22. KRISTJANSSON K; CHONG SS; VANDENVEYVER IB; SUBRAMANIAN S; SNABES MC; HUGHES MR
      PREIMPLANTATION SINGLE-CELL ANALYSES OF DYSTROPHIN GENE DELETIONS USING WHOLE GENOME AMPLIFICATION

      Nature genetics
    23. CHONG SS; EICHLER EE; NELSON DL; HUGHES MR
      ROBUST AMPLIFICATION AND ETHIDIUM-VISIBLE DETECTION OF THE FRAGILE-X-SYNDROME CGG REPEAT USING PFU POLYMERASE

      American journal of medical genetics
    24. SNABES MC; CHONG SS; SUBRAMANIAN SB; KRISTJANSSON K; DISEPIO D; HUGHES MR
      PREIMPLANTATION SINGLE-CELL ANALYSIS OF MULTIPLE GENETIC-LOCI BY WHOLE-GENOME AMPLIFICATION

      Proceedings of the National Academy of Sciences of the United Statesof America
    25. VANDENVEYVER IB; CHONG SS; KRISTJANSSON K; SNABES MC; MOISE KJ; HUGHES MR
      MOLECULAR ANALYSIS OF HUMAN PLATELET ANTIGEN SYSTEM-1 ANTIGEN ON SINGLE CELLS CAN BE APPLIED TO PREIMPLANTATION GENETIC DIAGNOSIS FOR PREVENTION OF ALLOIMMUNE THROMBOCYTOPENIA

      American journal of obstetrics and gynecology
    26. CHONG SS; KRISTJANSSON K; COTA J; HANDYSIDE AH; HUGHES MR
      PREIMPLANTATION PREVENTION OF X-LINKED DISEASE - RELIABLE AND RAPID SEX DETERMINATION OF SINGLE HUMAN-CELLS BY RESTRICTION ANALYSIS OF SIMULTANEOUSLY AMPLIFIED ZFX AND ZFY SEQUENCES

      Human molecular genetics
    27. CHONG SS; KRISTJANSSON K; ZOGHBI HY; HUGHES MR
      MOLECULAR-CLONING OF THE CDNA-ENCODING A HUMAN RENAL SODIUM-PHOSPHATETRANSPORT PROTEIN AND ITS ASSIGNMENT TO CHROMOSOME 6P21.3-P23

      Genomics
    28. CHONG SS; KRISTJANSSON K; VANDENVEYVER IB; SNABES MC; HUGHES MR
      PREIMPLANTATION ANALYSIS FOR DYSTROPHIN GENE DELETIONS AFTER SINGLE-CELL GENOME PREAMPLIFICATION

      American journal of human genetics
    29. VANDENVEYVER IB; CHONG SS; MOISE KJ; HUGHES MR
      A PREIMPLANTATION DIAGNOSTIC-APPROACH FOR THE PREVENTION OF NEONATAL ALLOIMMUNE THROMBOCYTOPENIC PURPURA

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 05/06/20 alle ore 16:08:45