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    1. Papadimitriou, G; Dikeos, D; Daskalopoulou, E; Karadima, G; Avramopoulos, D; Contis, C; Stefanis, C
      Association between GABA-A receptor alpha 5 subunit gene locus and schizophrenia of a later age of onset

      NEUROPSYCHOBIOLOGY
    2. Papadimitriou, GN; Dikeos, DG; Karadima, G; Avramopoulos, D; Daskalopoulou, EG; Stefanis, CN
      GABA-A receptor beta 3 and alpha 5 subunit gene cluster on chromosome 15q11-q13 and bipolar disorder: A genetic association study

      AMERICAN JOURNAL OF MEDICAL GENETICS
    3. Petersen, MB; Karadima, G; Samaritaki, M; Avramopoulos, D; Vassilopoulos, D; Mikkelsen, M
      Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    4. Barbi, G; Kennerknecht, I; Wohr, G; Avramopoulos, D; Karadima, G; Petersen, MB
      Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype

      AMERICAN JOURNAL OF MEDICAL GENETICS
    5. Panas, M; Avramopoulos, D; Karadima, G; Petersen, MB; Vassilopoulos, D
      Apolipoprotein E and presenilin-1 genotypes in Huntington's disease

      JOURNAL OF NEUROLOGY
    6. 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
    7. SAVAGE AR; PETERSEN MB; PETTAY D; TAFT L; ALLRAN K; FREEMAN SB; KARADIMA G; AVRAMOPOULOS D; TORFS C; MIKKELSEN M; HASSOLD TJ; SHERMAN SL
      ELUCIDATING THE MECHANISMS OF PATERNAL NONDISJUNCTION OF CHROMOSOME-21 IN HUMANS

      Human molecular genetics (Print)
    8. PAPADIMITRIOU GN; DIKEOS DG; KARADIMA G; AVRAMOPOULOS D; DASKALOPOULOU EG; VASSILOPOULOS D; STEFANIS CN
      ASSOCIATION BETWEEN THE GABA(A) RECEPTOR ALPHA(5) SUBUNIT GENE LOCUS (GABRA(5)) AND BIPOLAR AFFECTIVE-DISORDER

      American journal of medical genetics
    9. Panas, M; Karadimas, C; Avramopoulos, D; Vassilopoulos, D
      Central nervous system involvement in four patients with Charcot-Marie-Tooth disease with connexin 32 extracellular mutations

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    10. LAMB NE; FEINGOLD E; SAVAGE A; AVRAMOPOULOS D; FREEMAN S; GU Y; HALLBERG A; HERSEY J; KARADIMA G; PETTAY D; SAKER D; SHEN J; TAFT L; MIKKELSEN M; PETERSEN MB; HASSOLD T; SHERMAN SL
      CHARACTERIZATION OF SUSCEPTIBLE CHIASMA CONFIGURATIONS THAT INCREASE THE RISK FOR MATERNAL NONDISJUNCTION OF CHROMOSOME-21

      Human molecular genetics
    11. BARTSCH O; HINKEL GK; PETERSEN MB; KONIG U; BUGGE M; MIKKELSEN M; AVRAMOPOULOS D; MORRIS M; ANTONARAKIS SE
      A LARGE FAMILY WITH SUBTELOMERIC TRANSLOCATION T(18-21)(Q23-Q22.1) AND MOLECULAR BREAKPOINT IN THE DOWN-SYNDROME CRITICAL REGION

      Human genetics
    12. LAMB NE; PETTAY D; FREEMAN SB; PETERSON MB; TAFT L; HERSEY J; GU Y; AUSTIN AS; SHEN J; SAKER D; AVRAMOPOULOS D; MIKKELSEN M; HASSOLD TJ; SHERMAN SL
      EXAMINING THE RELATIONSHIP BETWEEN RECOMBINATION AND MATERNAL AGE-DEPENDENT NONDISJUNCTION - MOLECULAR STUDIES OF TRISOMY-21

      Cytogenetics and cell genetics
    13. PETERSEN MB; AVRAMOPOULOS D; VASSILOPOULOS D; GRIGORIADOU M; MIKKELSEN M
      IS APOLIPOPROTEIN-E ALLELE E4 A RISK FACTOR FOR DOWN-SYNDROME IN YOUNG MOTHERS

      Cytogenetics and cell 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. DIKEOS DG; AVRAMOPOULOS D; PAPADIMITRIOU GN; DASKALOPOULOU EG; KARADIMA G; STEFANIS CN
      ASSOCIATION BETWEEN DRD3 AND UNIPOLAR AFFECTIVE-DISORDER

      American journal of medical genetics
    16. PAPADIMITRIOU GN; KARADIMA G; DIKEOS DG; AVRAMOPOULOS D; DASKALOPOULOU EG; VASSILOPOULOS D; STEFANIS CN
      GABA-A RECEPTOR ALPHA-5 SUBUNIT GENE LOCUS - ASSOCIATION WITH BIPOLARILLNESS

      American journal of medical genetics
    17. SARRI C; GYFTODIMOU J; AVRAMOPOULOS D; GRIGORIADOU M; PEDERSEN W; PANDELIA E; PANGALOS C; ABAZIS D; KITSOS G; VASSILOPOULOS D; BRONDUMNIELSEN K; PETERSEN MB
      PARTIAL TRISOMY 17Q22-QTER AND PARTIAL MONOSOMY XQ27-QTER IN A GIRL WITH A DE-NOVO UNBALANCED TRANSLOCATION DUE TO A POSTZYGOTIC ERROR - CASE-REPORT AND REVIEW OF THE LITERATURE ON PARTIAL TRISOMY 17QTER

      American journal of medical genetics
    18. AVRAMOPOULOS D; KENNERKNECHT I; BARBI G; ECKERT D; DELABAR JM; MAUNOURY C; HALLBERG A; PETERSEN MB
      A CASE OF APPARENT TRISOMY-21 WITHOUT THE DOWNS-SYNDROME PHENOTYPE

      Journal of Medical Genetics
    19. SKLAVOUNOU E; ECONOMOUPETERSEN E; KARADIMA G; PANAS M; AVRAMOPOULOS D; VARSOU A; VASSILOPOULOS D; PETERSEN MB
      APOLIPOPROTEIN-E POLYMORPHISM IN THE GREEK POPULATION

      Clinical genetics
    20. 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
    21. PETERSEN MB; KARADIMA G; SAMARITAKI M; AVRAMOPOULOS D; VASSILOPOULOS D; MIKKELSEN M
      ASSOCIATION BETWEEN PRESENILIN-1 POLYMORPHISM AND MATERNAL MEIOSIS-IIERRORS IN DOWN-SYNDROME

      American journal of human genetics
    22. PANAS M; AVRAMOPOULOS D; KARADIMA G; PETERSEN MB; VASSILOPOULOS D
      APOLIPOPROTEIN-E AND PRESENILIN-1 GENOTYPES IN HUNTINGTON-DISEASE

      American journal of human genetics
    23. LAMB NE; FREEMAN SB; SAVAGEAUSTIN A; PETTAY D; TAFT L; HERSEY J; GU YC; SHEN J; SAKER D; MAY KM; AVRAMOPOULOS D; PETERSEN MB; HALLBERG A; MIKKELSEN M; HASSOLD TJ; SHERMAN SL
      SUSCEPTIBLE CHIASMATE CONFIGURATIONS OF CHROMOSOME-21 PREDISPOSE TO NONDISJUNCTION IN BOTH MATERNAL MEIOSIS-I AND MEIOSIS-II

      Nature genetics
    24. BUGGE M; BLENNOW E; FRIEDRICH U; PETERSEN MB; PEDEUTOUR F; TSEZOU A; ORUM A; HERMANN S; LYNGBYE T; SARRI C; AVRAMOPOULOS D; KITSIOU S; LAMBERT JC; GUZDA M; TOMMERUP N; BRONDUMNIELSEN K
      TETRASOMY 18P DE-NOVO - PARENTAL ORIGIN AND DIFFERENT MECHANISMS OF FORMATION (VOL 4, PG 160, 1996)

      European journal of human genetics
    25. BUGGE M; BLENNOW E; FRIEDRICH U; PETERSEN MB; PEDEUTOUR F; TSEZOU A; ORUM A; HERMANN S; LYNGBYE T; SARRI C; AVRAMOPOULOS D; KITSIOU S; LAMBERT JC; GUZDA M; TOMMERUP N; BRONDUMNIELSEN K
      TETRASOMY 18P DE-NOVO - PARENTAL ORIGIN AND DIFFERENT MECHANISMS OF FORMATION

      European journal of human genetics
    26. AVRAMOPOULOS D; MIKKELSEN M; VASSILOPOULOS D; GRIGORIADOU M; PETERSEN MB
      APOLIPOPROTEIN-E ALLELE DISTRIBUTION IN PARENTS OF DOWNS-SYNDROME CHILDREN

      Lancet
    27. AVRAMOPOULOS D; KITSOS G; ECONOMOUPETERSEN E; GRIGORIADOU M; VASSILOPOULOS D; PAPAGEORGIOU C; PSILAS K; PETERSEN MB
      EXCLUSION OF ONE PEDIGREE AFFECTED BY ADULT-ONSET PRIMARY OPEN-ANGLE GLAUCOMA FROM LINKAGE TO THE JUVENILE GLAUCOMA LOCUS ON CHROMOSOME 1Q21-Q31

      Journal of Medical Genetics
    28. TALBOT CC; AVRAMOPOULOS D; GERKEN S; CHAKRAVARTI A; ARMOUR JA; MATSUNAMI N; WHITE R; ANTONARAKIS SE
      THE TETRANUCLEOTIDE REPEAT POLYMORPHISM D21S1245 DEMONSTRATES HYPERMUTABILITY IN GERMLINE AND SOMATIC-CELLS

      Human molecular genetics
    29. AVRAMOPOULOS D; MIKKELSEN M; VASSILOPOULOS D; GRIGORIADOU M; PETERSEN MB
      CORRELATION BETWEEN HIGH-FREQUENCY OF APOLIPOPROTEIN-E ALLELE EPSILON-4 AND DECREASING MATERNAL AGE IN MOTHERS OF CHILDREN WITH DOWN-SYNDROME

      American journal of human genetics
    30. 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
    31. SARRI C; GYFTODIMOU J; AVRAMOPOULOS D; GRIGORIADOU M; PANDELIA E; PANGALOS C; ABAZI D; KITSOS G; VASSILOPOULOS D; BRONDUMNIELSEN K; PETERSEN MB
      PARTIAL TRISOMY 17Q22-QTER AND PARTIAL MONOSOMY XQ27-QTER IN A GIRL WITH A DE-NOVO UNBALANCED TRANSLOCATION DUE TO A POSTZYGOTIC ERROR

      American journal of human genetics
    32. CHEN HM; LOWTHER W; AVRAMOPOULOS D; ANTONARAKIS SE
      HOMOLOGOUS LOCI DXYS156X AND DXYS156Y CONTAIN A POLYMORPHIC PENTANUCLEOTIDE REPEAT (TAAAA)(N) AND MAP TO HUMAN X-CHROMOSOME AND Y-CHROMOSOME

      Human mutation
    33. PANGALOS C; AVRAMOPOULOS D
      UNDERSTANDING THE MECHANISM(S) OF MOSAIC TRISOMY-21 BY USING DNA POLYMORPHISM ANALYSIS (VOL 54, PG 473, 1994)

      American journal of human genetics
    34. PANGALOS C; AVRAMOPOULOS D; BLOUIN JL; RAOUL O; DEBLOIS MC; PRIEUR M; SCHINZEL AA; GIKA M; ABAZIS D; ANTONARAKIS SE
      UNDERSTANDING THE MECHANISM(S) OF MOSAIC TRISOMY-21 BY USING DNA POLYMORPHISM ANALYSIS

      American journal of human genetics
    35. TALBOT CC; WARREN AC; AVRAMOPOULOS D; ANTONARAKIS SE
      POLYMORPHIC DINUCLEOTIDE REPEATS AT THE D3S1417, D3S1418 AND D12S271 LOCI

      Human molecular genetics
    36. PETERSEN MB; ANTONARAKIS SE; HASSOLD TJ; FREEMAN SB; SHERMAN SL; AVRAMOPOULOS D; MIKKELSEN M
      PATERNAL NONDISJUNCTION IN TRISOMY-21 - EXCESS OF MALE-PATIENTS

      Human molecular genetics
    37. MCINNIS MG; CHAKRAVARTI A; BLASCHAK J; PETERSEN MB; SHARMA V; AVRAMOPOULOS D; BLOUIN JL; KONIG U; BRAHE C; MATISE TC; WARREN AC; TALBOT CC; VANBROECKHOVEN C; LITT M; ANTONARAKIS SE
      A LINKAGE MAP OF HUMAN CHROMOSOME-21 - 43 PCR MARKERS AT AVERAGE INTERVALS OF 2.5 CM

      Genomics
    38. BLOUIN JL; AVRAMOPOULOS D; PANGALOS C; ANTONARAKIS SE
      NORMAL PHENOTYPE WITH PATERNAL UNIPARENTAL ISODISOMY FOR CHROMOSOME-21

      American journal of human genetics
    39. TALBOT CC; AVRAMOPOULOS D; GERKEN S; BLASCHAK J; CHAKRAVARTI A; MATSUNAMI N; WHITE R; ANTONARAKIS SE
      A (AAAG)N POLYMORPHIC MARKER WITH EXTRAORDINARY HYPERMUTABILITY ON HUMAN CHROMOSOME-21

      American journal of human genetics
    40. PANGALOS C; AVRAMOPOULOS D; BLOUIN JL; RAOUL O; DEBLOIS MC; PRIEUR M; SCHINZEL A; GIKA M; ABAZIS D; ANTONARAKIS SE
      UNDERSTANDING THE MECHANISM(S) OF MOSAIC TRISOMY-21 USING DNA POLYMORPHISM ANALYSIS

      American journal of human genetics
    41. CHEN H; LOWTHER W; AVRAMOPOULOS D; ANTONARAKIS SE
      DXYS156 IS A POLYMORPHIC LOCUS DUE TO EXPANSION OF A (TAAAA) MOTIF WITHIN A LINE REPETITIVE ELEMENT

      American journal of human genetics
    42. BLOUIN JL; AVRAMOPOULOS D; PANGALOS C; ANTONARAKIS SE
      NORMAL PHENOTYPE WITH PATERNAL UNIPARENTAL ISODISOMY FOR CHROMOSOME-21

      American journal of human genetics
    43. ANTONARAKIS SE; BLOUIN JL; MAHER J; AVRAMOPOULOS D; THOMAS G; TALBOT CC
      MATERNAL UNIPARENTAL DISOMY FOR HUMAN CHROMOSOME-14, DUE TO LOSS OF ACHROMOSOME-14 FROM SOMATIC-CELLS WITH T(13 14) TRISOMY-14

      American journal of human genetics


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Documento generato il 06/08/20 alle ore 04:35:29