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La ricerca find articoli where authors phrase all words ' PUTNAM EA' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 10 riferimenti
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    1. Himelein, MJ; Putnam, EA
      Work activities of academic clinical psychologists: Do they practice what they teach?

      PROFESSIONAL PSYCHOLOGY-RESEARCH AND PRACTICE
    2. Guala, A; Danesino, C; Milewicz, DM; Putnam, EA; Franceschini, F
      The metacarpophalangeal profile in a family with congenital contractural arachnodactyly

      GENETIC COUNSELING
    3. Raghunath, M; Putnam, EA; Ritty, T; Hamstra, D; Park, ES; Tschodrich-Rotter, M; Peters, R; Rehemtulla, A; Milewicz, DM
      Carboxy-terminal conversion of profibrillin to fibrillin at a basic site by PACE/furin-like activity required for incorporation in the matrix

      JOURNAL OF CELL SCIENCE
    4. PARK ES; PUTNAM EA; CHITAYAT D; CHILD A; MILEWICZ DM
      CLUSTERING OF FBN2 MUTATIONS IN PATIENTS WITH CONGENITAL CONTRACTURALARACHNODACTYLY INDICATES AN IMPORTANT ROLE OF THE DOMAINS ENCODED BY EXONS 24 THROUGH 34 DURING HUMAN-DEVELOPMENT

      American journal of medical genetics
    5. PUTNAM EA; PARK ES; CHILD A; CHITAYAT D; MILEWICZ DM
      CLUSTERING OF FBN2 MUTATIONS IN PATIENTS WITH CONGENITAL CONTRACTURALARACHNODACTYLY (CCA)

      American journal of human genetics
    6. PUTNAM EA; PARK ES; AALFS CM; HENNEKAM RCM; MILEWICZ DM
      PARENTAL SOMATIC AND GERM-LINE MOSAICISM FOR A FBN2 MUTATION AND ANALYSIS OF FBN2 TRANSCRIPT LEVELS IN DERMAL FIBROBLASTS

      American journal of human genetics
    7. PUTNAM EA; CHO M; ZINN AB; TOWBIN JA; BYERS PH; MILEWICZ DM
      DELINEATION OF THE MARFAN PHENOTYPE ASSOCIATED WITH MUTATIONS IN EXONS 23-32 OF THE FBN1 GENE

      American journal of medical genetics
    8. PUTNAM EA; ZHANG H; RAMIREZ F; MILEWICZ DM
      FIBRILLIN-2 (FBN2) MUTATIONS RESULT IN THE MARFAN-LIKE DISORDER, CONGENITAL CONTRACTURAL ARACHNODACTYLY

      Nature genetics
    9. MILEWICZ DM; CHO M; ZINN AB; TOWBIN JA; BYERS PH; PUTNAM EA
      DELINEATION OF THE MARFAN PHENOTYPE ASSOCIATED WITH MUTATIONS IN EXONS 23 THROUGH 32 OF THE FBN1 GENE

      American journal of human genetics
    10. PUTNAM EA; MILEWICZ DM
      A MUTATION IN THE FBN2 GENE IN DERMAL FIBROBLASTS FROM A CONGENITAL CONTRACTURAL ARACHNODACTYLY PATIENT

      American journal of human genetics


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Documento generato il 29/10/20 alle ore 13:09:07