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La ricerca find articoli where authors phrase all words ' Goizet, C' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 9 riferimenti
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    1. Vital, A; Ferrer, X; Lagueny, A; Vandenberghe, A; Latour, P; Goizet, C; Canron, MH; Louiset, P; Petry, KG; Vital, C
      Histopathological features of X-linked Charcot-Marie-Tooth disease in 8 patients from 6 families with different connexin32 mutations

      JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
    2. Coupry, I; Taine, L; Goizet, C; Soriano, C; Mortemousque, B; Arveiler, B; Lacombe, D
      Leucodystrophy and oculocutaneous albinism in a child with an 11q14 deletion

      JOURNAL OF MEDICAL GENETICS
    3. Rodriguez, D; Gauthier, F; Bertini, E; Bugiani, M; Brenner, M; N'guyen, S; Goizet, C; Gelot, A; Surtees, R; Pedespan, JM; Hernandorena, X; Troncoso, M; Uziel, G; Messing, A; Ponsot, G; Pham-Dinh, D; Dautigny, A; Boespflug-Tanguy, O
      Infantile Alexander disease: Spectrum of GFAP mutations and genotype-phenotype correlation

      AMERICAN JOURNAL OF HUMAN GENETICS
    4. Goizet, C; Excoffier, E; Taine, L; Taupiac, E; El Moneim, AA; Arveiler, B; Bouvard, M; Lacombe, D
      Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH

      AMERICAN JOURNAL OF MEDICAL GENETICS
    5. Battin, J; Lacombe, D; Taine, L; Goizet, C
      Williams syndrome and behavioral phenotypes in human microdeletion syndromes

      BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE
    6. Goizet, C; Bonneau, D; Lacombe, D
      W syndrome: Report of three cases and review

      AMERICAN JOURNAL OF MEDICAL GENETICS
    7. TAINE L; GOIZET C; WEN ZQ; PETRIJ F; BREUNING MH; AYME S; SAURA R; ARVEILER B; LACOMBE D
      SUBMICROSCOPIC DELETION OF CHROMOSOME 16P13.3 IN PATIENTS WITH RUBINSTEIN-TAYBI-SYNDROME

      American journal of medical genetics
    8. TAINE L; GOIZET C; WEN ZQ; PETRIJ F; BREUNING M; SAURA R; ARVEILER B; LACOMBE D
      FREQUENCY OF 16P13.3 SUBMICROSCOPIC DELETIONS IN FRENCH PATIENTS WITHRUBINSTEIN-TAYBI-SYNDROME

      Cytogenetics and cell genetics
    9. TAINE L; GOIZET C; WEN ZQ; CHATEIL JF; BATTIN J; SAURA R; LACOMBE D
      18P MONOSOMY WITH MIDLINE DEFECTS AND A DE-NOVO SATELLITE IDENTIFIED BY FISH

      Annales de genetique


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/10/20 alle ore 01:03:56