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La ricerca find articoli where authors phrase all words ' HERTZ JM' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 26 riferimenti
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    1. Hertz, JM; Juncker, I; Persson, U; Matthijs, G; Schmidtke, J; Petersen, MB; Kjeldsen, M; Gregersen, N
      Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome

      HUMAN MUTATION
    2. Borglum, AD; Balslev, T; Haagerup, A; Birkebaek, N; Binderup, H; Kruse, TA; Hertz, JM
      A new locus for Seckel syndrome on chromosome 18p11.31-q11.2

      EUROPEAN JOURNAL OF HUMAN GENETICS
    3. Jais, JP; Knebelmann, B; Giatras, I; De Marchi, M; Rizzoni, G; Renieri, A; Weber, M; Gross, O; Netzer, KO; Flinter, F; Pirson, Y; Verellen, C; Wieslander, J; Persson, U; Tryggvason, K; Martin, P; Hertz, JM; Schroder, C; Sanak, M; Krejcova, S; Carvalho, MF; Saus, J; Antignac, C; Smeets, H; Gubler, MC
      X-linked Alport syndrome: Natural history in 195 families and genotype-phenotype correlations in males

      JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
    4. Haagerup, A; Hertz, JM; Christensen, MF; Binderup, H; Kruse, TA
      Cathepsin K gene mutations and 1q21 haplotypes in patients with pycnodysostosis in an outbred population

      EUROPEAN JOURNAL OF HUMAN GENETICS
    5. Kamperis, K; Siggaard, C; Herlin, T; Nathan, E; Hertz, JM; Rittig, S
      A novel splicing mutation in the V-2 vasopressin receptor

      PEDIATRIC NEPHROLOGY
    6. Hertz, JM; Schell, G; Doerfler, W
      Factors affecting de novo methylation of foreign DNA in mouse embryonic stem cells

      JOURNAL OF BIOLOGICAL CHEMISTRY
    7. MARTIN P; HEISKARI N; ZHOU J; LEINONEN A; TUMELIUS T; HERTZ JM; BARKER D; GREGORY M; ATKIN C; STYRKARSDOTTIR U; NEUMANN H; SPRINGATE J; SHOWS T; PETTERSSON E; TRYGGVASON K
      HIGH MUTATION DETECTION RATE IN THE COL4A5 COLLAGEN GENE IN SUSPECTEDALPORT-SYNDROME USING PCR AND DIRECT DNA-SEQUENCING

      Journal of the American Society of Nephrology
    8. KARADIMA G; BUGGE M; NICOLAIDIS P; VASSILOPOULOS D; AVRAMOPOULOS D; GRIGORIADOU M; ALBRECHT B; PASSARGE E; ANNEREN G; BLENNOW E; CLAUSEN N; GALLAVOUMVOURAKI A; TSEZOU A; KITSIOUTZELI S; HAHNEMANN JM; HERTZ JM; HOUGE G; KUKLIK M; MACEK M; LACOMBE D; MILLER K; MONCLA A; PAJARES IL; PATSALIS PC; PRIEUR M; VEKEMANS M; VONBEUST G; BRONDUMNIELSEN K; PETERSEN MB
      ORIGIN OF NONDISJUNCTION IN TRISOMY-8 AND TRISOMY-8 MOSAICISM

      European journal of human genetics
    9. BUGGE M; COLLINS A; PETERSEN MB; FISHER J; BRANDT C; HERTZ JM; TRANEBJAERG L; DELOZIERBLANCHET C; NICOLAIDES P; BRONDUMNIELSEN K; MORTON N; MIKKELSEN M
      NONDISJUNCTION OF CHROMOSOME-18

      Human molecular genetics
    10. HANSEN C; BUGGE M; BRANDT CA; HERTZ JM; TRANEBJOAERG L; MIKKELSEN M; PETERSEN MB
      APOLIPOPROTEIN-E ALLELES IN MOTHERS OF TRISOMY-18 CONCEPTUSES

      Clinical genetics
    11. HERTZ JM; HANSEN KN; JUNCKER I; KJELDSEN M; GREGERSEN N
      A NOVEL MISSENSE MUTATION (402C-]T) IN EXON-1 IN THE EDA GENE IN A FAMILY WITH X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA

      Clinical genetics
    12. VORECHOVSKY I; LUO LP; HERTZ JM; FROLAND SS; KLEMOLA T; FIORINI M; QUINTI I; PAGANELLI R; OZSAHIN H; HAMMARSTROM L; WEBSTER ADB; SMITH CIE
      MUTATION PATTERN IN BRUTON TYROSINE KINASE GENE IN 26 UNRELATED PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA

      Human mutation
    13. SCHWARTZ M; SORENSEN N; HANSEN FJ; HERTZ JM; NORBY S; TRANEBJAERG L; SKOVBY F
      QUANTIFICATION, BY SOLID-PHASE MINISEQUENCING, OF THE TELOMERIC AND CENTROMERIC COPIES OF THE SURVIVAL MOTOR-NEURON GENE IN FAMILIES WITH SPINAL MUSCULAR-ATROPHY

      Human molecular genetics
    14. KARADIMA G; AVRAMOPOULOS D; GRIGORIADOU M; PETERSEN MB; ALBRECHT B; ANNEREN G; BLENNOW E; BRONDUMNIELSEN K; BUGGE M; CLAUSEN N; GALLAVOUMVOURAKI A; HAHNEMANN JM; HERTZ JM; KITSIOUTZELI S; LACOMBE D; MILLER K; MONCLA A; PAJARES IL; PASSARGE E; PATSALIS PC; PRIEUR M; TSEZOU A; VASSILOPOULOS D; VEKEMANS M; VONBEUST G
      NONDISJUNCTION STUDIES IN TRISOMY-8

      Cytogenetics and cell genetics
    15. BUGGE M; HANSEN C; BRANDT CA; HERTZ JM; TRANEBJAERG L; MIKKELSEN M; PETERSEN MB
      APOLIPOPROTEIN-E ALLELES IN MOTHERS OF TRISOMY-18 CONCEPTUSES

      American journal of human genetics
    16. KARADIMA G; BUGGE M; NICOLAIDIS P; VASSILOPOULOS D; VONBEUST G; PAJARES IL; ALBRECHT B; ANNEREN G; AVRAMOPOULOS D; BLENNOW E; BRONDUMNIELSEN K; CLAUSEN N; GALLAVOUMVOURAKI A; GRIGORIADOU M; HAHNEMANN JM; HERTZ JM; KITSIOUTZELI S; LACOMBE D; MILLER K; MONCLA A; PASSARGE E; PATSALIS PC; PRIEUR M; TSEZOU A; VEKEMANS M; PETERSEN MB
      ORIGIN OF NONDISJUNCTION IN TRISOMY-8 AND TRISOMY-8 MOSAICISM

      American journal of human genetics
    17. WOLGIN DL; HERTZ JM
      EFFECTS OF ACUTE AND CHRONIC COCAINE ON MILK INTAKE, BODY-WEIGHT, ANDACTIVITY IN BOTTLE-FED AND CANNULA-FED RATS

      Behavioural pharmacology
    18. HERTZ JM; HEISKARI N; ZHOU J; JENSEN UB; TRYGGVASON K
      A NONSENSE MUTATION IN THE COL4A5 COLLAGEN GENE IN A FAMILY WITH X-LINKED JUVENILE ALPORT SYNDROME

      Kidney international
    19. HERTZ JM; HUANG HV
      EVOLUTION OF THE SINDBIS-VIRUS SUBGENOMIC MESSENGER-RNA PROMOTER IN CULTURED-CELLS

      Journal of virology
    20. HERTZ JM; HUANG HV
      HOST-DEPENDENT EVOLUTION OF THE SINDBIS-VIRUS PROMOTER FOR SUBGENOMICMESSENGER-RNA SYNTHESIS

      Journal of virology
    21. HERTZ JM; MARIYAMA M; THOMSEN A; REEDERS ST; KRUSE TA
      A TAQI AND A BAMHI POLYMORPHISM IN THE COL4A4 GENE ON CHROMOSOME 2Q35-37

      Clinical genetics
    22. HERTZ JM; TOMMERUP N; SORENSEN FB; HENRIQUES UV; NIELSEN A; THERKELSEN AJ
      PARTIAL DELETION 11Q - REPORT OF A CASE WITH A LARGE TERMINAL DELETION 11Q21-QTER WITHOUT LOSS OF TELOMERIC SEQUENCES, AND REVIEW OF THE LITERATURE

      Clinical genetics
    23. GRIGORIADOU M; BUGGE M; AVRAMOPOULOS D; KITSIOUTZELI S; ANNEREN G; HERTZ JM; LACOMBE D; TSEZOU A; GALLAVOUMVOURAKI A; CLAUSEN N; VASSILOPOULOS D; BRONDUMNIELSEN K; PETERSEN MB
      NONDISJUNCTION STUDIES IN TRISOMY-8

      American journal of human genetics
    24. FLINT TJ; HERTZ JM; KRUSE TA
      A LINKAGE MAP OF HUMAN-CHROMOSOME-2

      Cytogenetics and cell genetics
    25. HERTZ JM; BORGLUM AD; BRANDT CA; FLINT T; BISGAARD C
      CHARCOT-MARIE-TOOTH DISEASE TYPE 1A - THE PARENTAL ORIGIN OF A DE-NOVO 17P11.2-P12 DUPLICATION

      Clinical genetics
    26. KRUSE TA; FLINT T; REEDERS ST; HERTZ JM
      GENETIC-MAPPING OF ALPP, CGC, COL4A3 AND COL4A4, 4 GENES LOCATED AT THE DISTAL PART OF CHROMOSOME-2Q

      Cytogenetics and cell genetics


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Documento generato il 25/05/20 alle ore 11:05:06