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La ricerca find articoli where authors phrase all words ' Ferrero, GB' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 26 riferimenti
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    1. Martini, G; Riva, P; Rabbia, F; Molini, V; Ferrero, GB; Cerutti, F; Carra, R; Veglio, F
      Heart rate variability in childhood obesity

      CLINICAL AUTONOMIC RESEARCH
    2. Bamford, RN; Roessler, E; Burdine, RD; Saplakoglu, U; dela Cruz, J; Splitt, M; Goodship, JA; Towbin, J; Bowers, P; Ferrero, GB; Marino, B; Schier, AF; Shen, MM; Muenke, M; Casey, B
      Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects (vol 26, pg 365, 2000)

      NATURE GENETICS
    3. Ponzone, A; Spada, M; Ferrero, GB; Ponzone, R; Ferraris, S
      Newborn feeding and screening for phenylketonuria

      ACTA PAEDIATRICA
    4. GEBBIA M; BASSI MT; FERRERO GB; KOSAKI K; CASEY B
      MOLECULAR-GENETICS OF HUMAN LEFT-RIGHT AXIS MALFORMATIONS

      Modern pathology
    5. GEBBIA M; FERRERO GB; PILIA G; BASSI MT; AYLSWORTH AS; PENMANSPLITT M; BIRD LM; BAMFORTH JS; BURN J; SCHLESSINGER D; NELSON DL; CASEY B
      X-LINKED SITUS ABNORMALITIES RESULT FROM MUTATIONS IN ZIC3

      Nature genetics
    6. GEBBIA M; BASSI MT; FERRERO GB; KOSAKI K; CASEY B
      CLINICAL AND MOLECULAR-GENETICS OF HUMAN LEFT-RIGHT AXIS DISORDERS

      Molecular biology of the cell
    7. GEBBIA M; BASSI MT; FERRERO GB; KOSAKI K; CASEY B
      MULTIGENIC MUTATIONS ASSOCIATED WITH COMPLEX HEART MALFORMATIONS AND RELATED SITUS ABNORMALITIES

      The American journal of pathology
    8. CASEY B; GEBBIA M; FERRERO GB; PILIA G; YAMADA M; AYLSWORTH AS; PENMANSPLITT M; BIRD LM; BAMFORTH JS; BURN J; SCHLESSINGER D; NELSON DL
      SITES INVERSUS, HEART-DEFECTS, AND OTHER MANIFESTATIONS OF X-LINKED HETEROTAXY CAUSED BY MUTATIONS IN THE ZINC-FINGER TRANSCRIPTION FACTOR ZIC3

      American journal of human genetics
    9. FERRERO GB; GEBBIA M; PILIA G; WITTE D; PEIER A; HOPKIN RJ; CRAIGEN WJ; SHAFFER LG; SCHLESSINGER D; BALLABIO A; CASEY B
      A SUBMICROSCOPIC DELETION IN XQ26 ASSOCIATED WITH FAMILIAL SITUS AMBIGUUS

      American journal of human genetics
    10. SPADA M; FERRARIS S; FERRERO GB; SARTORE M; LANZA C; PERFETTO F; DESANCTIS L; DOMPE C; BLAU N; PONZONE A
      MONITORING TREATMENT IN TETRAHYDROBIOPTERIN DEFICIENCY BY SERUM PROLACTIN

      Journal of inherited metabolic disease
    11. MACKENZIE JJ; FITZPATRICK J; BABYN P; FERRERO GB; BALLABIO A; BILLINGSLEY G; BULMAN DE; STRASBERG P; RAY PN; COSTA T
      X-LINKED SPONDYLOEPIPHYSEAL DYSPLASIA - A CLINICAL, RADIOLOGICAL, ANDMOLECULAR STUDY OF A LARGE KINDRED

      Journal of Medical Genetics
    12. FERRERO GB; FRANCO B; ROTH EJ; FIRULLI BA; BORSANI G; DELMASMATA J; WEISSENBACH J; HALLEY G; SCHLESSINGER D; CHINAULT AC; ZOGHBI HY; NELSON DL; BALLABIO A
      AN INTEGRATED PHYSICAL AND GENETIC-MAP OF A 35 MB REGION ON CHROMOSOME XP22.3-XP21.3

      Human molecular genetics
    13. WANG I; FRANCO B; FERRERO GB; CHINAULT AC; WEISSENBACH J; CHUMAKOV I; LEPASLIER D; LEVILLIERS J; KLINK A; RAPPOLD GA; BALLABIO A; PETIT C
      HIGH-DENSITY PHYSICAL MAPPING OF A 3-MB REGION IN XP22.3 AND REFINED LOCALIZATION OF THE GENE FOR X-LINKED RECESSIVE CHONDRODYSPLASIA PUNCTATA (CDPX1)

      Genomics
    14. FERRARIS S; SPADA M; FERRERO GB; DOMPE C; PONZONE A
      CHYLOMICRONEMIA SYNDROME DUE TO LIPOPROTE IN-LIPASE (LPL) DEFICIENCY - A POSSIBLE CAUSE OF METABOLIC EMERGENCY

      Rivista italiana di pediatria
    15. YEN PH; FERRERO GB; CHINAULT AC; MOHANDAS T; BALLABIO A
      CHARACTERIZATION OF THE DELETION BREAKPOINTS IN A PATIENT WITH STEROID SULFATASE DEFICIENCY

      Human mutation
    16. VANSLEGTENHORST MA; BASSI MT; BORSANI G; WAPENAAR MC; FERRERO GB; DECONCILIIS L; RUGARLI EI; GRILLO A; FRANCO B; ZOGHBI HY; BALLABIO A
      A GENE FROM THE XP22.3 REGION SHARES HOMOLOGY WITH VOLTAGE-GATED CHLORIDE CHANNELS

      Human molecular genetics
    17. SCHAEFER L; WAPENAAR MC; BASSI MT; FERRERO GB; GRILLO A; ROTH RJ; BALLABIO A; ZOGHBI HY
      CHARACTERIZATION AND CLONING OF THE CRITICAL REGION FOR THE MICROPHTHALMIA WITH LINEAR SKIN DEFECTS SYNDROME (MLS)

      Journal of cellular biochemistry
    18. FERRERO GB; FRANCO B; ROTH EJ; FIRULLI BA; GRILLO A; BORSANI G; CHINAULT AC; NELSON DL; ZOGHBI HY; BALLABIO A
      AN INTEGRATED 40-MB PHYSICAL MAP OF THE DISTAL SHORT ARM OF THE HUMANX-CHROMOSOME

      Cytogenetics and cell genetics
    19. LINDSAY EA; GRILLO A; FERRERO GB; ROTH EJ; MAGENIS E; GROMPE M; HULTEN M; GOULD C; BALDINI A; ZOGHBI HY; BALLABIO A
      MICROPHTHALMIA WITH LINEAR SKIN DEFECTS (MLS) SYNDROME - CLINICAL, CYTOGENETIC, AND MOLECULAR CHARACTERIZATION

      American journal of medical genetics
    20. SCHAEFER L; FERRERO GB; GRILLO A; BASSI MT; ROTH EJ; WAPENAAR MC; VANOMMEN GJB; MOHANDAS TK; ROCCHI M; ZOGHBI HY; BALLABIO A
      A HIGH-RESOLUTION DELETION MAP OF HUMAN CHROMOSOME-XP22

      Nature genetics
    21. WAPENAAR MC; BASSI MT; SCHAEFER L; GRILLO A; FERRERO GB; CHINAULT AC; BALLABIO A; ZOGHBI HY
      THE GENES FOR X-LINKED OCULAR ALBINISM (OA1) AND MICROPHTHALMIA WITH LINEAR SKIN DEFECTS (MLS) - CLONING AND CHARACTERIZATION OF THE CRITICAL REGIONS

      Human molecular genetics
    22. LEE WC; FERRERO GB; CHINAULT AC; YEN PH; BALLABIO A
      A YEAST ARTIFICIAL CHROMOSOME CONTIG LINKING THE STEROID SULFATASE AND KALLMANN SYNDROME LOCI ON THE HUMAN X-CHROMOSOME SHORT ARM

      Genomics
    23. BALLABIO A; SCHAEFER L; FERRERO GB; GRILLO A; BASSI MT; ROTH EJ; WAPENAAR MC; VANOMMEN GJB; MOHANDAS TK; ROCCHI M; NELSON D; ZOGHBI HY
      A HIGH-RESOLUTION 30-MB DELETION MAP OF THE DISTAL SHORT ARM OF THE HUMAN X-CHROMOSOME

      Cytogenetics and cell genetics
    24. FERRERO GB; SCHAEFER L; GRILLO A; BASSI MT; ROTH EJ; WAPENAAR MC; VANOMMEN GJB; MOHANDAS TK; ROCCHI M; CHINAULT AC; NELSON D; ZOGHBI HY; BALLABIO A
      A HIGH-RESOLUTION 30-MEGABASE DELETION MAP OF THE DISTAL SHORT ARM OFTHE HUMAN X-CHROMOSOME

      American journal of human genetics
    25. WAPENAAR MC; BASSI MT; SCHAEFER L; GRILLO A; FERRERO GB; CHINAULT AC; BALLABIO A; ZOGHBI HY
      THE GENES FOR MICROPHTHALMIA WITH LINEAR SKIN DEFECTS (MLS) AND X-LINKED OCULAR ALBINISM (OA1) - CLONING AND CHARACTERIZATION OF THE CRITICAL REGIONS

      American journal of human genetics
    26. LEE WC; FERRERO GB; CHINAULT AC; YEN PH; BALLABIO A
      A YEAST ARTIFICIAL CHROMOSOME CONTIG LINKING THE STEROID SULFATASE AND KALLMANN SYNDROME LOCI ON THE HUMAN X-CHROMOSOME SHORT ARM

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 07/06/20 alle ore 06:08:31