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La ricerca find articoli where soggetti phrase all words 'ITALIAN FAMILIES' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 11 riferimenti
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    1. Schelhaas, HJ; Ippe, PF; Hageman, G; Sinke, RJ; van der Laan, EN; Beemer, FA
      Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxia

      JOURNAL OF NEUROLOGY
    2. Zhou, YX; Qiao, WH; Gu, WH; Xie, H; Tang, BS; Zhou, LS; Yang, BX; Takiyama, Y; Tsuji, S; He, HY; Deng, CX; Goldfarb, LG; Wang, GX
      Spinocerebellar ataxia type 1 in China - Molecular analysis and genotype-phenotype correlation in 5 families

      ARCHIVES OF NEUROLOGY
    3. D'Alfonso, S; Nistico, L; Bocchio, D; Bomprezzi, R; Marrosu, MG; Murru, MR; Lai, M; Massacesi, L; Ballerini, C; Repice, A; Salvetti, M; Montesperelli, C; Ristori, G; Trojano, M; Liguori, M; Gambi, D; Quattrone, A; Tosi, R; Momigliano-Richiardi, P
      An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population

      JOURNAL OF NEUROVIROLOGY
    4. Villanova, M; Mercuri, E; Bertini, E; Sabatelli, P; Morandi, L; Mora, M; Sewry, C; Brockington, M; Brown, SC; Ferreiro, A; Maraldi, NM; Toda, T; Guicheney, P; Merlini, L; Muntoni, F
      Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndrome

      NEUROMUSCULAR DISORDERS
    5. Thongnoppakhun, W; Wilairat, P; Vareesangthip, K; Yenchitsomanus, P
      Long RT-PCR amplification of the entire coding sequence of the polycystic kidney disease 1 (PKD1) Gene

      BIOTECHNIQUES
    6. D'Andrea, E; Montagna, M; Menin, C; Santacatterina, M; Chieco-Bianchi, L
      BRCA genes and ovarian neoplasia

      TUMORI
    7. HALL JG; SOLEHDIN F
      GENETICS OF NEURAL-TUBE DEFECTS

      Mental retardation and developmental disabilities research reviews (Print)
    8. FABRIZI GM; SIMONATI A; MORBIN M; CAVALLARO T; TAIOLI F; BENEDETTI MD; EDOMI P; RIZZUTO N
      CLINICAL AND PATHOLOGICAL CORRELATIONS IN CHARCOT-MARIE-TOOTH NEUROPATHY TYPE 1A WITH THE 17P11.2P12 DUPLICATION - A CROSS-SECTIONAL MORPHOMETRIC AND IMMUNOHISTOCHEMICAL STUDY IN 20 CASES

      Muscle & nerve
    9. ARRIGONI A; BARGIACCHI S; BENATTI P; HEOUAINE A; MARENI C; MESSERINI L; MONTERA MP; MORI S; PERCESEPE A; PRESCIUTTINI S; ROCCI MP; SALA P
      COLLECTION OF ITALIAN HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER (HNPCC) PEDIGREES

      Tumori
    10. DEVRIES DD; WENT LN; BRUYN GW; SCHOLTE HR; HOFSTRA RMW; BOLHUIS PA; VANOOST BA
      GENETIC AND BIOCHEMICAL IMPAIRMENT OF MITOCHONDRIAL COMPLEX-I ACTIVITY IN A FAMILY WITH LEBER HEREDITARY OPTIC NEUROPATHY AND HEREDITARY SPASTIC DYSTONIA

      American journal of human genetics
    11. KAPLAN NL; HILL WG; WEIR BS
      LIKELIHOOD METHODS FOR LOCATING DISEASE GENES IN NONEQUILIBRIUM POPULATIONS

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 13/08/20 alle ore 14:43:13