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La ricerca find articoli where authors phrase all words 'Nolin, SL' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 16 riferimenti
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    1. Brown, WT; Nolin, SL
      Apparent FMR1 allele instability in non-Fragile X males - Invited commentary

      GENETIC TESTING
    2. Crawford, DC; Schwartz, CE; Meadows, KL; Newman, JL; Taft, LF; Gunter, C; Brown, WT; Carpenter, NJ; Howard-Peebles, PN; Monaghan, KG; Nolin, SL; Reiss, AL; Feldman, GL; Rohlfs, EM; Warren, ST; Sherman, SL
      Survey of the fragile X syndrome CGG repeat and the short-tendem-repeat and single-nucleotide-polymorphism haplotypes in an African American population

      AMERICAN JOURNAL OF HUMAN GENETICS
    3. Allingham-Hawkins, SJ; Babul-Hirji, R; Chitayat, D; Holden, JJA; Yang, KT; Lee, C; Hudson, R; Gorwill, H; Nolin, SL; Glicksman, A; Jenkins, EC; Brown, WT; Howard-Peebles, PN; Becchi, C; Cummings, E; Fallon, L; Seitz, S; Black, SH; Vianna-Morgante, AM; Costa, SS; Otto, PA; Mingroni-Netto, RC; Murray, A; Webb, J; MacSwinney, F; Dennis, N; Jacobs, PA; Syrrou, M; Georgiou, I; Patsalis, PC; Uzielli, MLG; Guarducci, S; Lapi, E; Cecconi, A; Ricci, U
      Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study - Preliminary data

      AMERICAN JOURNAL OF MEDICAL GENETICS
    4. Dobkin, C; Ding, XH; Li, SY; Houck, G; Nolin, SL; Glicksman, A; Zhong, N; Jenkins, EC; Brown, WT
      Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection

      AMERICAN JOURNAL OF MEDICAL GENETICS
    5. Jenkins, EC; Wen, GY; Kim, KS; Zhong, N; Sapienza, VJ; Hong, H; Chen, J; Li, SY; Houck, GE; Ding, XH; Nolin, SL; Dobkin, CS; Brown, WT
      Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies

      AMERICAN JOURNAL OF MEDICAL GENETICS
    6. Nolin, SL; Houck, GE; Gargano, AD; Blumstein, H; Dobkin, CS; Brown, WT
      FMR1 CCG-repeat instability by single sperm and lymphocytes of fragile-X premutation males

      AMERICAN JOURNAL OF HUMAN GENETICS
    7. ASHLEYKOCH AE; ROBINSON H; GLICKSMAN AE; NOLIN SL; SCHWARTZ CE; BROWN WT; TURNER G; SHERMAN SL
      EXAMINATION OF FACTORS ASSOCIATED WITH INSTABILITY OF THE FMR1 CGG REPEAT

      American journal of human genetics
    8. ASHLEY AE; ROBINSON H; GLICKSMAN AE; NOLIN SL; SCHWARTZ C; BROWN WT; TURNER G; SHERMAN SL
      IDENTIFICATION OF RISK-FACTORS ASSOCIATED WITH INSTABILITY OF THE FMR1 CGG REPEAT

      American journal of human genetics
    9. NOLIN SL; HOUCK GE; BLUMSTEIN H; YE LL; DOBKIN CS; BROWN WT
      SINGLE-CELL ANALYSIS SHOWS DIFFERENT FMR1 CGG REPEAT STABILITY IN SPERM AND LYMPHOCYTES OF PREMUTATION MALES

      American journal of human genetics
    10. DOBKIN CS; NOLIN SL; COHEN I; SUDHALTER V; BIALER MG; DING XH; JENKINS EC; ZHONG N; BROWN WT
      TISSUE DIFFERENCES IN FRAGILE-X MOSAICS - MOSAICISM IN BLOOD-CELLS MAY DIFFER GREATLY FROM SKIN

      American journal of medical genetics
    11. COHEN IL; NOLIN SL; SUDHALTER V; DING XH; DOBKIN CS; BROWN WT
      MOSAICISM FOR THE FMR1 GENE INFLUENCES ADAPTIVE SKILLS DEVELOPMENT INFRAGILE X-AFFECTED MALES

      American journal of medical genetics
    12. NOLIN SL; LEWIS FA; YE LL; HOUCK GE; GLICKSMAN AE; LIMPRASERT P; LI SY; ZHONG N; ASHLEY AE; FEINGOLD E; SHERMAN SL; BROWN WT
      FAMILIAL TRANSMISSION OF THE FMR1 CGG REPEAT

      American journal of human genetics
    13. NOLIN SL; GLICKSMAN A; LEWIS FA; YE LL; HOUCK GE; ASHLEY AE; SHERMAN SL; BROWN WT
      EVIDENCE FOR A FAMILIAL FACTOR INVOLVED IN CGG REPEAT EXPANSION IN FRAGILE-X SYNDROME

      American journal of human genetics
    14. DOBKIN CS; NOLIN SL; COHEN J; SUDHALTER V; BIALER MG; DING XH; JENKINS EC; ZHONG N; BROWN WT
      DIFFERENCES BETWEEN MOSAICISM IN BLOOD-CELLS AND SKIN FIBROBLASTS SUGGEST THAT SHIN MAY BETTER PREDICT BRAIN-FUNCTION

      American journal of human genetics
    15. NOLIN SL; GLICKSMAN A; HOUCK GE; BROWN WT; DOBKIN CS
      MOSAICISM IN FRAGILE-X AFFECTED MALES

      American journal of medical genetics
    16. NOLIN SL; HOUCK GE; LI SY; DING XH; BROWN WT; DOBKIN CS
      MOSAICISM IN FRAGILE-X AFFECTED MALES

      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 12:39:11