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La ricerca find articoli where authors phrase all words ' Whiteford, ML' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 18 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. Tobias, ES; Patrick, WJA; MacKenzie, JR; Whiteford, ML
      A case of Acro-renal-mandibular syndrome in an 18 week male fetus

      CLINICAL DYSMORPHOLOGY
    3. Tyson, J; Tranebjaerg, L; McEntagart, M; Larsen, LA; Christiansen, M; Whiteford, ML; Bathen, J; Aslaksen, B; Sorland, SJ; Lund, O; Pembrey, ME; Malcolm, S; Bitner-Glindzicz, M
      Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen (vol 107, pg 499, 2000)

      HUMAN GENETICS
    4. Tyson, J; Tranebjaerg, L; McEntagart, M; Larsen, LA; Christiansen, M; Whiteford, ML; Bathen, J; Aslaksen, B; Sorland, SJ; Lund, O; Pembrey, ME; Malcolm, S; Bitner-Glindzicz, M
      Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen

      HUMAN GENETICS
    5. Reid, E; Dearlove, AM; Whiteford, ML; Rhodes, M; Rubinsztein, DC
      Autosomal dominant spastic paraplegia - Refined SPG8 locus and additional genetic heterogeneity

      NEUROLOGY
    6. Tobias, ES; Morrison, N; Whiteford, ML; Tolmie, JL
      Towards earlier diagnosis of 22q11 deletions

      ARCHIVES OF DISEASE IN CHILDHOOD
    7. FLEMING CJ; SINCLAIR DU; WHITE EJ; WINCHESTER B; WHITEFORD ML; CONNOR JM
      A FUCOSIDOSIS PATIENT WITH RELATIVE LONGEVITY AND A MISSENSE MUTATIONIN EXON-7 OF THE ALPHA-FUCOSIDASE GENE

      Journal of inherited metabolic disease
    8. OH J; HO LL; ALAMELLO S; AMATO D; ARMSTRONG L; BELLUCCI S; CARAKUSHANSKY G; ELLIS JP; FONG CT; GREEN JS; HEON E; LEGIUS E; LEVIN AV; NIEUWENHUIS HK; PINCKERS A; TAMURA N; WHITEFORD ML; YAMASAKI H; SPRITZ RA
      MUTATION ANALYSIS OF PATIENTS WITH HERMANSKY-PUDLAK-SYNDROME - A FRAMESHIFT HOT-SPOT IN THE HPS GENE AND APPARENT LOCUS HETEROGENEITY

      American journal of human genetics
    9. WHITEFORD ML; NARENDRA A; WHITE MP; COOKE A; WILKINSON AG; ROBERTSON KJ; TOLMIE JL
      PATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME-6 CAUSES TRANSIENT NEONATAL DIABETES

      Journal of Medical Genetics
    10. DAVIDSON HR; RENWICK A; DOUGLAS SF; IRVINE LA; WHITEFORD ML; CROW Y; BLACK D; TRAINER AH
      EXPERIENCE OF BRCA1 2 MUTATION TESTING IN THE WEST OF SCOTLAND - RESULTS AND CLINICAL IMPLICATIONS/

      Journal of Medical Genetics
    11. SHIELD JPH; GARDNER RJ; WADSWORTH EJK; WHITEFORD ML; JAMES RS; ROBINSON DO; BAUM JD; TEMPLE IK
      ETIOPATHOLOGY AND GENETIC-BASIS OF NEONATAL DIABETES

      Archives of Disease in Childhood
    12. DAVIDSON HR; RENWICK AA; DOUGLAS SF; IRVINE L; WHITEFORD ML; CROW Y; BLACK D; TRAINER AH
      MUTATION ANALYSIS OF BRCA1 AND BRCA2 - WHAT DO THE RESULTS MEAN

      American journal of human genetics
    13. WHITEFORD ML; TOLMIE JL
      HOLOPROSENCEPHALY IN THE WEST OF SCOTLAND 1975-1994

      Journal of Medical Genetics
    14. WHITEFORD ML; COUTTS J; ALROOMI L; MATHER A; LOWTHER G; COOKE A; VAUGHAN JI; MOORE GE; TOLMIE JL
      UNIPARENTAL ISODISOMY FOR CHROMOSOME-16 IN A GROWTH-RETARDED INFANT WITH CONGENITAL HEART-DISEASE

      Prenatal diagnosis
    15. WHITEFORD ML; WILKINSON JD; MCCOLL JH; CONLON FM; MICHIE JR; EVANS TJ; PATON JY
      OUTCOME OF BURKHOLDERIA (PSEUDOMONAS) CEPACIA COLONIZATION IN CHILDREN WITH CYSTIC-FIBROSIS FOLLOWING A HOSPITAL OUTBREAK

      Thorax
    16. WILSON SM; WHITEFORD ML; PLUMB JA; BOVELL DL
      ANION (I-125(-)) EFFLUX FROM OSMOTICALLY SWOLLEN HUMAN OVARIAN ADENOCARCINOMA CELLS - EFFECTS OF P-GLYCOPROTEIN EXPRESSION

      Journal of physiology
    17. WILSON SM; WHITEFORD ML; BOVELL DL; PEDIANI JD; KO WH; SMITH GL; LEE CM; ELDER HY
      THE REGULATION OF MEMBRANE I-125(-) AND RB-86(-CELL LINE (NCL-SG3) DERIVED FROM THE HUMAN SWEAT GLAND EPITHELIUM() PERMEABILITY IN A VIRALLY TRANSFORMED)

      Experimental physiology
    18. WHITEFORD ML; BOVELL DL; PEDIANI JD; SMITH GL; ELDER HY; LEE CM; WILSON SM
      THE REGULATION OF CHLORIDE PERMEABILITY BY ATP IN A CELL-LINE (NCL-SG3) ESTABLISHED FROM THE HUMAN SWEAT GLAND EPITHELIUM

      Journal of physiology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/10/20 alle ore 12:08:29