Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where authors phrase all words ' FORREST SM' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 27 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Van Agtmael, T; Forrest, SM; Williamson, R
      Genes for left-handedness: How to search for the needle in the haystack?

      LATERALITY
    2. Wangerek, LA; Dahl, HHM; Senden, TJ; Carlin, JB; Jans, DA; Dunstan, DE; Ioannou, PA; Williamson, R; Forrest, SM
      Atomic force microscopy imaging of DNA - cationic liposome complexes optimised for gene transfection into neuronal cells

      JOURNAL OF GENE MEDICINE
    3. Forrest, SM; Knight, M; Akerman, BR; Cashman, JR; Treacy, EP
      A novel deletion in the flavin-containing monooxygenase gene (FMO3) in a Greek patient with trimethylaminuria

      PHARMACOGENETICS
    4. Hand, PJ; Gardner, RJM; Knight, MA; Forrest, SM; Storey, E
      Clinical features of a large Australian pedigree with episodic ataxia type1

      MOVEMENT DISORDERS
    5. Storey, E; Gardner, RJM; Knight, MA; Kennerson, ML; Tuck, RR; Forrest, SM; Nicholson, GA
      A new autosomal dominant pure cerebellar ataxia

      NEUROLOGY
    6. Storey, E; du Sart, D; Shaw, JH; Lorentzos, P; Kelly, L; Gardner, RJM; Forrest, SM; Biros, I; Nicholson, GA
      Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    7. Cashman, JR; Akerman, BR; Forrest, SM; Treacy, EP
      Population-specific polymorphisms of the human FMO3 gene: Significance fordetoxication

      DRUG METABOLISM AND DISPOSITION
    8. Massie, J; du Sart, D; Forshaw, K; Carlin, J; Forrest, SM
      The relationship between neonatal immunoreactive trypsinogen, Delta F508, and IVS8-5T

      JOURNAL OF MEDICAL GENETICS
    9. Delatycki, MB; Williamson, R; Forrest, SM
      Friedreich ataxia: an overview

      JOURNAL OF MEDICAL GENETICS
    10. Smith, MJ; Gardner, RJM; Knight, MA; Forrest, SM; Beyreuther, K; Storey, E; McLean, CA; Cotton, RGH; Cappal, R; Masters, CL
      Early-onset Alzheimer's disease caused by a novel mutation at codon 219 ofthe presenilin-1 gene

      NEUROREPORT
    11. Delatycki, MB; Camakaris, J; Brooks, H; Evans-Whipp, T; Thorburn, DR; Williamson, R; Forrest, SM
      Direct evidence that mitochondrial iron accumulation occurs in Friedreich ataxia

      ANNALS OF NEUROLOGY
    12. Delatycki, MB; Knight, M; Koenig, M; Cossee, M; Williamson, R; Forrest, SM
      G130V, a common FRDA point mutation, appears to have arisen from a common founder

      HUMAN GENETICS
    13. Delatycki, MB; Paris, DBBP; Gardner, RJM; Nicholson, GA; Nassif, N; Storey, E; MacMillan, JC; Collins, V; Williamson, R; Forrest, SM
      Clinical and genetic study of Friedreich ataxia in an Australian population

      AMERICAN JOURNAL OF MEDICAL GENETICS
    14. Ramus, SJ; Forrest, SM; Pitt, DD; Cotton, RGH
      Genotype and intellectual phenotype in untreated phenylketonuria patients

      PEDIATRIC RESEARCH
    15. Storey, E; Forrest, SM; Shaw, JH; Mitchell, P; Gardner, RJM
      Spinocerebellar ataxia type 2 - Clinical features of a pedigree displayingprominent frontal-executive dysfunction

      ARCHIVES OF NEUROLOGY
    16. Biros, I; Forrest, SM
      Duplex PCR for autosomal dominant spinocerebellar ataxia testing: A nonradioactive rapid screening method

      MOLECULAR DIAGNOSIS
    17. TREACY EP; AKERMAN BR; CHOW LML; YOUIL R; BIBEAU C; LIN J; BRUCE AG; KNIGHT M; DANKS DM; CASHMAN JR; FORREST SM
      MUTATIONS OF THE FLAVIN-CONTAINING MONOOXYGENASE GENE (FMO3) CAUSE TRIMETHYLAMINURIA, A DEFECT IN DETOXICATION

      Human molecular genetics
    18. DELATYCKI MB; PARIS D; GARDNER RJM; FORSHAW K; NICHOLSON GA; NASSIF N; WILLIAMSON R; FORREST SM
      SPERM DNA ANALYSIS IN A FRIEDREICH ATAXIA PREMUTATION CARRIER SUGGESTS BOTH MEIOTIC AND MITOTIC EXPANSION IN THE FRDA GENE

      Journal of Medical Genetics
    19. SHEFFIELD LJ; OSBORN AH; HUTCHISON WM; SILLENCE DO; FORREST SM; WHITE SJ; DAHL HHM
      SEGREGATION OF MUTATIONS IN ARYLSULFATASE-E AND CORRELATION WITH THE CLINICAL PRESENTATION OF CHONDRODYSPLASIA PUNCTATA

      Journal of Medical Genetics
    20. FORREST SM; DELATYCKI M; PARIS D; GARDNER RJM; FORSHAW K; NICHOLSON G; NASSIS N; WILLIAMSON R
      THE FRIEDREICH ATAXIA MUTATION MAY ORIGINATE FROM A PREMUTATION AND SHOWS SIZE-REDUCTION WHEN TRANSMITTED FROM PARENT TO AFFECTED CHILD

      American journal of human genetics
    21. LAGERSTROMFERMER M; SUNDVALL M; JOHNSEN E; WARNE GL; FORREST SM; ZAJAC JD; RICKARDS A; RAVINE D; LANDEGREN U; PETTERSSON U
      X-LINKED RECESSIVE PANHYPOPITUITARISM ASSOCIATED WITH A REGIONAL DUPLICATION IN XQ25-Q26

      American journal of human genetics
    22. DISTANTE S; NASIOULAS S; SOMERS GR; CAMERON DJS; YOUNG MA; FORREST SM; GARDNER RJM
      FAMILIAL ADENOMATOUS POLYPOSIS IN A 5-YEAR-OLD CHILD - A CLINICAL, PATHOLOGICAL, AND MOLECULAR-GENETIC STUDY

      Journal of Medical Genetics
    23. SLATER H; SHAW JH; BANKIER A; FORREST SM; DAWSON G
      UPD-13 - NO INDICATION OF MATERNAL OR PATERNAL IMPRINTING OF GENES ONCHROMOSOME-13

      Journal of Medical Genetics
    24. SLATER H; SHAW JH; DAWSON G; BANKIER A; FORREST SM
      MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME-13 IN A PHENOTYPICALLY NORMAL-CHILD

      Journal of Medical Genetics
    25. RAMUS SJ; FORREST SM; PITT DB; SALEEBA JA; COTTON RGH
      COMPARISON OF GENOTYPE AND INTELLECTUAL PHENOTYPE IN UNTREATED PKU PATIENTS

      Journal of Medical Genetics
    26. COTTON RGH; RAMUS SJ; FORREST SM; PITT DB
      GENOTYPE CANNOT BE USED TO ACCURATELY PREDICT THE INTELLECTUAL PHENOTYPE OF UNTREATED PHENYLKETONURIA (PKU) PATIENTS

      American journal of human genetics
    27. FORREST SM; MAKRIS GS; COTTON RGH; YOUIL R; KEMPER B; SULLIVAN LJ; LOUGHNAN MS
      IDENTIFICATION OF MUTATIONS IN THE RHODOPOSIN GENE USING ILLEGITIMATETRANSCRIPTION

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 05/06/20 alle ore 23:59:43