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 soggetti phrase all words 'DNA testing' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 39 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Gasser, T; Dichgans, M; Finsterer, J; Hausmanowa-Petrusewicz, I; Jurkat-Rott, K; Klopstock, T; Leguern, E; Lehesjoki, AE; Lehmann-Horn, F; Lynch, T; Morris, H; Rossor, M; Steinlein, OK; Wood, N; Zaremba, J; Zeviani, M; Zoharn, A
      EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - Second of two parts

      EUROPEAN JOURNAL OF NEUROLOGY
    2. Gasser, T; Dichgans, M; Finsterer, J; Hausmanowa-Petrusewicz, I; Jurkat-Rott, K; Klopstock, T; LeGuern, E; Lehesjoki, AE; Lehmann-Horn, F; Lynch, T; Morris, H; Rossor, M; Steinlein, OK; Wood, N; Zaremba, J; Zeviani, M; Zoharn, A
      EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - First of two parts

      EUROPEAN JOURNAL OF NEUROLOGY
    3. Honda, K; Tun, Z; Young, D; Terao, T
      Examination of Y-STR mutations in sex chromosomal abnormality in forensic cases

      FORENSIC SCIENCE INTERNATIONAL
    4. Bach, G; Tomczak, J; Risch, N; Ekstein, J
      Tay-sachs screening in the Jewish Ashkenazi population: DNA testing is thepreferred procedure

      AMERICAN JOURNAL OF MEDICAL GENETICS
    5. Yu, S; Poulos, V; Stewart, P
      A novel mutation in a family with non-erythroid variant form of acute intermittent porphyria

      JOURNAL OF HUMAN GENETICS
    6. Motulsky, AG; Beutler, E
      Population screening in hereditary hemochromatosis

      ANNUAL REVIEW OF PUBLIC HEALTH
    7. Pulst, SM
      Ethical issues in DNA testing

      MUSCLE & NERVE
    8. Mihalov, JJ; Marderosian, AD; Pierce, JC
      DNA identification of commercial ginseng samples

      JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
    9. Baldauf, JJ; Ritter, J
      Management of low grade squamous intraepithelial lesion

      CONTRACEPTION FERTILITE SEXUALITE
    10. Wilcken, B; Travert, G
      Neonatal screening for cystic fibrosis: present and future

      ACTA PAEDIATRICA
    11. Hermeren, G
      Neonatal screening: ethical aspects

      ACTA PAEDIATRICA
    12. Zdenek, H; Lukac, J; Jabor, A; Chvalova, M; Voracek, J; Brozkova, H
      Human papillomavirus deoxyribonucleic acid testing in screening of high grade cervical intraepithelial neoplasia

      SAUDI MEDICAL JOURNAL
    13. Balazic, J; Zupanic, I
      Quality control and quality assurance in DNA laboratories: legal, civil and ethical aspects

      FORENSIC SCIENCE INTERNATIONAL
    14. Bird, TD
      Risks and benefits of DNA testing for neurogenetic disorders

      SEMINARS IN NEUROLOGY
    15. Decruyenaere, M; Evers-Kiebooms, G; Boogaerts, A; Cassiman, JJ; Cloostermans, T; Demyttenaere, K; Dom, R; Fryns, JP
      Psychological functioning before predictive testing for Huntington's disease: the role of the parental disease, risk perception, and subjective proximity of the disease

      JOURNAL OF MEDICAL GENETICS
    16. Whittaker, MH; Farkas, DH; Kaul, KL; Shrimpton, AE; Leonard, DGB
      Association for molecular pathology statement - Recommendations for in-house development and operation of molecular diagnostic tests

      AJCP. American journal of clinical pathology
    17. AMOS J; GOLD B
      TESTING ENVIRONMENT FOR SINGLE-GENE DISORDERS IN US REFERENCE LABORATORIES

      Human mutation
    18. KISHI M; TSUKADA T; SHIMIZU S; FUTAMI H; ITO Y; KANBE M; OBARA T; YAMAGUCHI K
      A LARGE GERMLINE DELETION OF THE MEN1 GENE IN A FAMILY WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-1

      Japanese journal of cancer research
    19. EGAWA S; FUTAMI H; TAKASAKI K; IIHARA M; OKAMOTO T; KANBE M; OHI T; SAIO Y; MIYAUCHI A; TAKIYAMA Y; KOGA M; MIYANAGA K; INOUE K; MITSUYAMA S; NOMURA Y; TAKEI H; MUGIYA S; ISHIDA O; ZEZE F; SHAKUTSUI S; INOUE H; OYA H; YOSHIMURA A; ISHIZUKA S; TSUJINO T; OBARA T; YAMAGUCHI K
      GENOTYPE-PHENOTYPE CORRELATION OF PATIENTS WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-2 IN JAPAN

      Japanese Journal of Clinical Oncology
    20. DUDOKDEWIT AC; TIBBEN A; DUIVENVOORDEN HJ; NIERMEIJER MF; PASSCHIER J
      PREDICTING ADAPTATION TO PRESYMPTOMATIC DNA TESTING FOR LATE-ONSET DISORDERS - WHO WILL EXPERIENCE DISTRESS

      Journal of Medical Genetics
    21. SHIMIZU S; TSUKADA T; FUTAMI H; UI K; KAMEYA T; KAWANAKA M; UCHIYAMA S; AOKI A; YASUDA H; KAWANO S; ITO Y; KANBE M; OBARA T; YAMAGUCHI K
      GERMLINE MUTATIONS OF THE MEN1 GENE IN JAPANESE KINDRED WITH MULTIPLEENDOCRINE NEOPLASIA TYPE-1

      Japanese journal of cancer research
    22. LITWIN CM; HILL HR
      SEROLOGIC AND DNA-BASED TESTING FOR CONGENITAL AND PERINATAL INFECTIONS

      The Pediatric infectious disease journal
    23. VANTSPIJKER A; TENKROODE HFJ
      PSYCHOLOGICAL-ASPECTS OF GENETIC-COUNSELING - A REVIEW OF THE EXPERIENCE WITH HUNTINGTONS-DISEASE

      Patient education and counseling
    24. GALJAARD H
      GENE TECHNOLOGY AND SOCIAL ACCEPTANCE

      Pathologie et biologie
    25. PAULSON GW; PRIOR TW
      ISSUES RELATED TO DNA TESTING FOR HUNTINGTONS-DISEASE IN SYMPTOMATIC PATIENTS

      Seminars in neurology
    26. GREGG RG; SIMANTEL A; FARRELL PM; KOSCIK R; KOSOROK MR; LAXOVA A; LAESSIG R; HOFFMAN G; HASSEMER D; MISCHLER EH; SPLAINGARD M
      NEWBORN SCREENING FOR CYSTIC-FIBROSIS IN WISCONSIN - COMPARISON OF BIOCHEMICAL AND MOLECULAR METHODS

      Pediatrics
    27. EVANS DGR; MAHER ER; MACLEOD R; DAVIES DR; CRAUFURD D
      UPTAKE OF GENETIC TESTING FOR CANCER PREDISPOSITION

      Journal of Medical Genetics
    28. DUDOKDEWIT AC; TIBBEN A; DUIVENVOORDEN HJ; FRETS PG; ZOETEWEIJ MW; LOSEKOOT M; VANHAERINGEN A; NIERMEIJER MF; PASSCHIER J; LINDHOUT D; MEIJERSHEIJBOER EJ; LODDER LN; TRIJSBURG RW; KLIJN JGM; BROCKERVRIENDS A; HELDERMAN ATJM; HILHORSTHOFSTEE Y; KANT S; MAATKIEVIT JA; OOSTERWIJK JC; VANDERSMAGT JJ; VEGTERVANDERVLIS M; VRIESVANDERWEERD MACS; BAKKER E; CORNELISSE CJ; DEVILEE P; TOPS C; VASEN HFA
      PSYCHOLOGICAL DISTRESS IN APPLICANTS FOR PREDICTIVE DNA TESTING FOR AUTOSOMAL-DOMINANT, HERITABLE, LATE-ONSET DISORDERS

      Journal of Medical Genetics
    29. MELLERIO JE; DUNNILL MGS; ALLISON W; ASHTON GHS; CHRISTIANO AM; UITTO J; EADY RAJ; MCGRATH JA
      RECURRENT MUTATIONS IN THE TYPE-VII COLLAGEN GENE (COL7A1) IN PATIENTS WITH RECESSIVE DYSTROPHIC EPIDERMOLYSIS-BULLOSA

      Journal of investigative dermatology
    30. VNENCAKJONES CL; PHILLIPS JA; JANCO RL; COHEN MP; DUPONT WD; KAZAZIAN HH; ROSSITER JP
      ANALYSIS OF FACTOR-VIII GENE INVERSION MUTATIONS IN 166 UNRELATED HEMOPHILIA-A FAMILIES - FREQUENCY AND UTILITY IN GENETIC-COUNSELING

      Haemophilia
    31. NAYFIELD SG
      ETHICAL AND SCIENTIFIC CONSIDERATIONS FOR CHEMOPREVENTION RESEARCH INCOHORTS AT GENETIC RISK FOR BREAST-CANCER

      Journal of cellular biochemistry
    32. SPENCE WC; BLACK SH; FALLON L; MADDALENA A; CUMMINGS E; MENAPACEDREW G; BICK DP; LEVINSON G; SCHULMAN JD; HOWARDPEEBLES PN
      MOLECULAR FRAGILE-X SCREENING IN NORMAL-POPULATIONS

      American journal of medical genetics
    33. WHITELAW S; NORTHOVER JM; HODGSON SV
      ATTITUDES TO PREDICTIVE DNA TESTING IN FAMILIAL ADENOMATOUS POLYPOSIS

      Journal of Medical Genetics
    34. POWELL RL; NORMAN HD; COWAN CM
      RELATIONSHIP OF BOVINE LEUKOCYTE ADHESION DEFICIENCY WITH GENETIC MERIT FOR PERFORMANCE TRAITS

      Journal of dairy science
    35. GRACE MB; BUZARD GS; WEINTRAUB BD
      ALLELE-SPECIFIC ASSOCIATED POLYMORPHISM ANALYSIS - NOVEL MODIFICATIONOF SSCP FOR MUTATION DETECTION IN HETEROZYGOUS ALLELES USING THE PARADIGM OF RESISTANCE TO THYROID-HORMONE

      Human mutation
    36. SHAGINA I; DADALI HL; SITNIKOV VP; PUGACHEV VV; MALYGINA NA; EVGRAFOV OV
      PRENATAL-DIAGNOSIS OF SPINAL MUSCULAR-ATROPHY IN RUSSIA

      Prenatal diagnosis
    37. RICHART RM
      SCREENING - THE NEXT CENTURY

      Cancer
    38. RONA RJ; BEECH R; MANDALIA S; DONNAI D; KINGSTON H; HARRIS R; WILSON O; AXTELL C; SWAN AV; KAVANAGH F
      THE INFLUENCE OF GENETIC-COUNSELING IN THE ERA OF DNA TESTING ON KNOWLEDGE, REPRODUCTIVE INTENTIONS AND PSYCHOLOGICAL WELL-BEING

      Clinical genetics
    39. HAYASHI K; YANDELL DW
      HOW SENSITIVE IS PCR-SSCP

      Human mutation


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 11/08/20 alle ore 15:58:09