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La ricerca find articoli where soggetti phrase all words 'Myhre syndrome' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 15 riferimenti
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    1. Whiteford, ML; Doig, WB; Raine, PAM; Hollman, AS; Tolmie, JL
      A new case of Myhre syndrome

      CLINICAL DYSMORPHOLOGY
    2. Wanner, M; Celebi, JT; Peacocke, M
      Identification of a PTEN mutation in a family with Cowden syndrome and Bannayan-Zonana syndrome

      JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY
    3. Titomanlio, L; Marzano, MG; Rossi, E; D'Armiento, M; De Brasi, D; Vega, GR; Andreucci, MV; Orsini, AVM; Santoro, L; Sebastio, G
      Case of Myhre syndrome with autism and peculiar skin histological findings

      AMERICAN JOURNAL OF MEDICAL GENETICS
    4. Stratakis, CA
      Genetics of Carney complex and related familial lentiginoses, and other multiple tumor syndromes

      PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
    5. Stratakis, CA
      Genetics of Carney complex and related familial lentiginoses, and other multiple tumor syndromes

      FRONTIERS IN BIOSCIENCE
    6. Otto, LR; Boriack, RL; Marsh, DJ; Kum, JB; Eng, C; Burlina, AB; Bennett, MJ
      Long-chain L 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency does not appear to be the primary cause of lipid myopathy in patients with Bannayan-Riley-Ruvalcaba syndrome (ERRS)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    7. TSUCHIYA KD; WIESNER G; CASSIDY SB; LIMWONGSE C; BOYLE JT; SCHWARTZ S
      DELETION 10Q23.2-Q23.33 IN A PATIENT WITH GASTROINTESTINAL JUVENILE POLYPOSIS AND OTHER FEATURES OF A COWDEN-LIKE SYNDROME

      Genes, chromosomes & cancer
    8. DILIBERTI JH
      INHERITED MACROCEPHALY-HAMARTOMA SYNDROMES

      American journal of medical genetics
    9. Zori, RT; Marsh, DJ; Graham, GE; Marliss, EB; Eng, C
      Germline PTEN mutation in a family with Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    10. FARRELL SA
      MICROPHTHALMIA, MARKED SHORT STATURE, HEARING-LOSS, AND DEVELOPMENTALDELAY - EXTENSION OF THE PHENOTYPE OF GOMBO SYNDROME

      American journal of medical genetics
    11. ARCH EM; GOODMAN BK; VANWESEP RA; LIAW D; CLARKE K; PARSONS R; MCKUSICK VA; GERAGHTY MT
      DELETION OF PTEN IN A PATIENT WITH BANNAYAN-RILEY-RUVALCABA-SYNDROME SUGGESTS ALLELISM WITH COWDEN-DISEASE

      American journal of medical genetics
    12. FARGNOLI MC; ORLOW SJ; SEMELCONCEPCION J; BOLOGNIA JL
      CLINICOPATHOLOGICAL FINDINGS IN THE BANNAYAN-RILEY-RUVALCABA-SYNDROME

      Archives of dermatology
    13. HARNED RK; BUCK JL; SOBIN LH
      THE HAMARTOMATOUS POLYPOSIS SYNDROMES - CLINICAL AND RADIOLOGIC FEATURES

      American journal of roentgenology
    14. FRYBURG JS; PELEGANO JP; BENNETT MJ; BEBIN EM
      LONG-CHAIN 3-HYDROXYACYL-COENZYME-A DEHYDROGENASE (L-CHAD) DEFICIENCYIN A PATIENT WITH THE BANNAYAN-RILEY-RUVALCABA-SYNDROME

      American journal of medical genetics
    15. GARCIACRUZ D; FIGUERA LE; FERIAVELAZCO A; SANCHEZCORONA J; GARCIACRUZ MO; RAMIREZDUENAS RM; HERNANDEZCORDOVA A; RUIZ MX; BITARALATORRE WE; RAMIREZDUENAS ML; CANTU JM
      THE MYHRE SYNDROME - REPORT OF 2 CASES

      Clinical genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 07/08/20 alle ore 03:08:06