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    1. Kenneson, A; Warren, ST
      The female and the fragile X reviewed

      SEMINARS IN REPRODUCTIVE MEDICINE
    2. Crawford, DC; Acuna, JM; Sherman, SL
      FMR1 and the fragile X syndrome: Human genome epidemiology review

      GENETICS IN MEDICINE
    3. Hagerman, RJ; Hagerman, PJ
      Fragile X syndrome: A model of gene-brain-behavior relationships

      MOLECULAR GENETICS AND METABOLISM
    4. Hegde, MR; Fawkner, M; Chong, B; McGaughran, J; Gilbert, D; Love, DR
      Compound heterozygosity at the FMR1 gene

      GENETIC TESTING
    5. Tzeng, CC; Lin, SJ; Chen, YJ; Kuo, PL; Jong, YJ; Tsai, LP; Chen, RM
      An effective strategy of using molecular testing to screen mentally retarded individuals for fragile X syndrome

      DIAGNOSTIC MOLECULAR PATHOLOGY
    6. Bontekoe, CJM; Bakker, CE; Nieuwenhuizen, IM; van der Linde, H; Lans, H; de Lange, D; Hirst, MC; Oostra, BA
      Instability of a (CGG)(98) repeat in the Fmr1 promoter

      HUMAN MOLECULAR GENETICS
    7. Kenneson, A; Zhang, FP; Hagedorn, CH; Warren, ST
      Reduced FMRP and increased FMR1 transcription is proportionally associatedwith CGG repeat number in intermediate-length and premutation carriers

      HUMAN MOLECULAR GENETICS
    8. Eliez, S; Feinstein, C
      The fragile X syndrome: bridging the gap from gene to behavior

      CURRENT OPINION IN PSYCHIATRY
    9. Bennetto, L; Pennington, BF; Porter, D; Taylor, AK; Hagerman, RJ
      Profile of cognitive functioning in women with the fragile X mutation

      NEUROPSYCHOLOGY
    10. Weinhausel, A; Haas, OA
      Evaluation of the fragile X (FRAXA) syndrome with methylation-sensitive PCR

      HUMAN GENETICS
    11. Simon, JA; Keenan, JM; Pennington, BF; Taylor, AK; Hagerman, RJ
      Discourse processing in women with fragile X syndrome: Evidence for a deficit establishing coherence

      COGNITIVE NEUROPSYCHOLOGY
    12. Johnston, C; Eliez, S; Dyer-Friedman, J; Hessl, D; Glaser, B; Blasey, C; Taylor, A; Reiss, A
      Neurobehavioral phenotype in carriers of the fragile X premutation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    13. Hegde, MR; Chong, B; Fawkner, M; Lambiris, N; Peters, H; Kenneson, A; Warren, ST; Love, DR; McGaughran, J
      Microdeletion in the FMR-1 gene: an apparent null allele using routine clinical PCR amplification

      JOURNAL OF MEDICAL GENETICS
    14. Saha, S; Karmakar, P; Chatterjee, C; Banerjee, D; Das, S; Dasgupta, UB
      Fragile X syndrome in Calcutta, India

      ANNALS OF CLINICAL BIOCHEMISTRY
    15. Kooy, RF; Willemsen, R; Oostra, BA
      Fragile X syndrome at the turn of the century

      MOLECULAR MEDICINE TODAY
    16. Tzountzouris, J; Kennedy, D; Skuterud, M; Connolly-Wilson, M; Holden, JJA; Lin, CC; Mak-Tam, E; Somerville, MJ; Summers, AM; Allingham-Hawkins, DJ
      Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: Implications for molecular diagnosis of the Fragile X syndrome

      GENETIC TESTING
    17. Gold, B; Radu, D; Balanko, A; Chiang, CS
      Diagnosis of Fragile X syndrome by Southern blot hybridization using a chemiluminescent probe: A laboratory protocol

      MOLECULAR DIAGNOSIS
    18. Mazzocco, MMM
      Advances in research on the fragile X syndrome

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    19. Tzeng, CC; Tzeng, PY; Sun, HS; Chen, RM; Lin, SJ
      Implication of screening for FMR1 and FMR2 gene mutation in individuals with nonspecific mental retardation in Taiwan

      DIAGNOSTIC MOLECULAR PATHOLOGY
    20. Irwin, SA; Galvez, R; Greenough, WT
      Dendritic spine structural anomalies in fragile-X mental retardation syndrome

      CEREBRAL CORTEX
    21. Crawford, DC; Wilson, B; Sherman, SL
      Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR

      HUMAN MOLECULAR GENETICS
    22. de Vries, BBA; Oostra, BA
      The fragile X syndrome: A model for mental retardation

      NEUROSCIENCE RESEARCH COMMUNICATIONS
    23. Genc, B; Muller-Hartmann, H; Zeschnigk, M; Deissler, H; Schmitz, B; Majewski, F; von Gontard, A; Doerfler, W
      Methylation mosaicism of 5 '-(CGG)(n)-3 ' repeats in fragile X, premutation and normal individuals

      NUCLEIC ACIDS RESEARCH
    24. Pesso, R; Berkenstadt, H; Cuckle, H; Gak, E; Peleg, L; Frydman, M; Barkai, G
      Screening for fragile X syndrome in women of reproductive age

      PRENATAL DIAGNOSIS
    25. Tassone, F; Hagerman, RJ; Chamberlain, WD; Hagerman, PJ
      Transcription of the FMR1 gene in individuals with fragile X syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    26. Bardoni, B; Mandel, JL; Fisch, GS
      FMR1 gene and fragile X syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    27. Tassone, F; Hagerman, RJ; Taylor, AK; Mills, JB; Harris, SW; Gane, LW; Hagerman, PJ
      Clinical involvement and protein expression in individuals with the FMR1 premutation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    28. Willemsen, R; Olmer, R; Otero, YD; Oostra, BA
      Twin sisters, monozygotic with the fragile X mutation, but with a different phenotype

      JOURNAL OF MEDICAL GENETICS
    29. Sheldon, L; Turk, J
      Monozygotic boys with fragile X syndrome

      DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
    30. White, PJ; Borts, RH; Hirst, MC
      Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism

      MOLECULAR AND CELLULAR BIOLOGY
    31. Sermon, K; Seneca, S; Vanderfaeillie, A; Lissens, W; Joris, H; Vandervorst, M; Van Steirteghem, A; Liebaers, I
      Preimplantation diagnosis for fragile X syndrome based on the detection ofthe non-expanded paternal and maternal CGG

      PRENATAL DIAGNOSIS
    32. Kaufmann, WE; Reiss, AL
      Molecular and cellular genetics of fragile X syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    33. Sun, YJ; Baumer, A
      Nonrandom X inactivation and selection of fragile X full mutation in fetalfibroblasts

      AMERICAN JOURNAL OF MEDICAL GENETICS
    34. Schmucker, B; Seidel, J
      Mosaicism for a full mutation and a normal size allele in two fragile X males

      AMERICAN JOURNAL OF MEDICAL GENETICS
    35. Petek, E; Kroisel, PM; Schuster, M; Zierler, H; Wagner, K
      Mosaicism in a fragile X male including a de novo deletion in the FMR1 gene

      AMERICAN JOURNAL OF MEDICAL GENETICS
    36. Taylor, AK; Tassone, F; Dyer, PN; Hersch, SM; Harris, JB; Greenough, WT; Hagerman, RJ
      Tissue heterogeneity of the FMR1 mutation in a high-functioning male with fragile X syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    37. Tassone, F; Hagerman, RJ; Gane, LW; Taylor, AK
      Strong similarities of the FMR1 mutation in multiple tissues: Postmortem studies of a male with a full mutation and a male carrier of a premutation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    38. Tassone, F; Hagerman, RJ; Ikle, DN; Dyer, PN; Lampe, M; Willemsen, R; Oostra, BA; Taylor, AK
      FMRP expression as a potential prognostic indicator in fragile X syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    39. Holden, JJA; Percy, M; Allingham-Hawkins, D; Brown, WT; Chiurazzi, P; Fisch, G; Gane, L; Gunter, C; Hagerman, R; Jenkins, EC; Kooy, RF; Lubs, HA; Murray, A; Neri, G; Schwartz, C; Tranebjaerg, L; Villard, L; Willems, PJ
      Eighth International Workshop on the Fragile X Syndrome and X-linked Mental Retardation, August 16-22, 1997

      AMERICAN JOURNAL OF MEDICAL GENETICS
    40. Kaufmann, WE; Abrams, MT; Chen, WM; Reiss, AL
      Genotype, molecular phenotype, and cognitive phenotype: Correlations in fragile X syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    41. Jenkins, EC; Wen, GY; Kim, KS; Zhong, N; Sapienza, VJ; Hong, H; Chen, J; Li, SY; Houck, GE; Ding, XH; Nolin, SL; Dobkin, CS; Brown, WT
      Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies

      AMERICAN JOURNAL OF MEDICAL GENETICS
    42. Abrams, MT; Kaufmann, WE; Rousseau, F; Oostra, BA; Wolozin, B; Taylor, CV; Lishaa, N; Morel, ML; Hoogeveen, A; Reiss, AL
      FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    43. Helderman-van den Enden, ATJM; Maaswinkel-Mooij, PD; Hoogendoorn, E; Willemsen, R; Maat-Kievit, JA; Losekoot, M; Oostra, BA
      Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities

      JOURNAL OF MEDICAL GENETICS
    44. de Vries, BBA; van den Boer-van den Berg, HMA; Niermeijer, MF; Tibben, A
      Dilemmas in Counselling females with the fragile X syndrome

      JOURNAL OF MEDICAL GENETICS
    45. Tassone, F; Longshore, J; Zunich, J; Steinbach, P; Salat, U; Taylor, AK
      Tissue-specific methylation differences in a fragile X premutation carrier

      CLINICAL GENETICS
    46. Nolin, SL; Houck, GE; Gargano, AD; Blumstein, H; Dobkin, CS; Brown, WT
      FMR1 CCG-repeat instability by single sperm and lymphocytes of fragile-X premutation males

      AMERICAN JOURNAL OF HUMAN GENETICS
    47. Willemsen, R; Anar, B; Otero, YD; de Vries, BBA; Hilhorst-Hofstee, Y; Smits, A; van Looveren, E; Willems, PJ; Galjaard, H; Oostra, BA
      Noninvasive test for fragile X syndrome, using hair root analysis

      AMERICAN JOURNAL OF HUMAN GENETICS
    48. Feldman, GL; Monaghan, KG
      Fragile X syndrome: A review of the molecular and clinical features

      JOURNAL OF CLINICAL LIGAND ASSAY
    49. RIDDLE JE; CHEEMA A; SOBESKY WE; GARDNER SC; TAYLOR AK; PENNINGTON BF; HAGERMAN RJ
      PHENOTYPIC INVOLVEMENT IN FEMALES WITH THE FMR1 GENE MUTATION

      American journal of mental retardation
    50. FEINSTEIN C; REISS AL
      AUTISM - THE POINT-OF-VIEW FROM FRAGILE-X STUDIES

      Journal of autism and developmental disorders
    51. 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
    52. DEVRIES BBA; HALLEY DJJ; OOSTRA BA; NIERMEIJER MF
      THE FRAGILE-X-SYNDROME

      Journal of Medical Genetics
    53. ASHLEYKOCH AE; ROBINSON H; GLICKSMAN AE; NOLIN SL; SCHWARTZ CE; BROWN WT; TURNER G; SHERMAN SL
      EXAMINATION OF FACTORS ASSOCIATED WITH INSTABILITY OF THE FMR1 CGG REPEAT

      American journal of human genetics
    54. CHAKRABARTI L; DAVIES KE
      FRAGILE-X-SYNDROME

      Current opinion in neurology
    55. ABBEDUTO L; HAGERMAN RJ
      LANGUAGE AND COMMUNICATION IN FRAGILE-X-SYNDROME

      Mental retardation and developmental disabilities research reviews
    56. OOSTRA BA; HOOGEVEEN AT
      ANIMAL-MODEL FOR FRAGILE-X-SYNDROME

      Annals of medicine
    57. MAZZOCCO MMM; KATES WR; BAUMGARDNER TL; FREUND LS; REISS AL
      AUTISTIC BEHAVIORS AMONG GIRLS WITH FRAGILE-X-SYNDROME

      Journal of autism and developmental disorders
    58. MAZZOCCO MMM; REISS AL
      NORMAL VARIATION IN SIZE OF THE FMR1 GENE IS NOT ASSOCIATED WITH VARIATION IN INTELLECTUAL-PERFORMANCE

      Intelligence
    59. HAMMOND LS; MACIAS MM; TARLETON JC; PAI GS
      FRAGILE-X-SYNDROME AND DELETIONS IN FMR1 - NEW CASE AND REVIEW OF THELITERATURE

      American journal of medical genetics
    60. MINGRONINETTO RC; PAVANELLO RCM; OTTO PA; VIANNAMORGANTE AM
      EXPERIENCE WITH MOLECULAR AND CYTOGENETIC DIAGNOSIS OF FRAGILE-X-SYNDROME IN BRAZILIAN FAMILIES

      Brazilian journal of genetics
    61. HAGERMAN RJ
      FRAGILE-X-SYNDROME - MOLECULAR AND CLINICAL INSIGHTS AND TREATMENT ISSUES

      Western journal of medicine
    62. VANRIJN MA; DEVRIES BBA; TIBBEN A; VANDENOUWELAND AMW; HALLEY DJJ; NIERMEIJER MF
      DNA TESTING FOR FRAGILE-X-SYNDROME - IMPLICATIONS FOR PARENTS AND FAMILY

      Journal of Medical Genetics
    63. LOESCH DZ; PETROVIC V; FRANCIS DI; OERTEL R; SLATER H
      REDUCTION OF CGG TRINUCLEOTIDE EXPANSION FROM MOTHER TO OFFSPRING IN 7 FRAGILE-X FAMILIES

      Clinical genetics
    64. GRONSKOV K; HJALGRIM H; BJERAGER MO; BRONDUMNIELSEN K
      DELETION OF ALL CGG REPEATS PLUS FLANKING SEQUENCES IN FMR1 DOES NOT ABOLISH GENE-EXPRESSION

      American journal of human genetics
    65. MORNET E; CHATEAU C; TAILLANDIER A; SIMONBOUY B; SERRE JL
      RECURRENT AND UNEXPECTED SEGREGATION OF THE FMR1 CGG REPEAT IN A FAMILY WITH FRAGILE-X SYNDROME

      Human genetics
    66. SHERMAN SL; MEADOWS KL; ASHLEY AE
      EXAMINATION OF FACTORS THAT INFLUENCE THE EXPANSION OF THE FRAGILE-X MUTATION IN A SAMPLE OF CONCEPTUSES FROM KNOWN CARRIER FEMALES

      American journal of medical genetics
    67. DOBKIN CS; NOLIN SL; COHEN I; SUDHALTER V; BIALER MG; DING XH; JENKINS EC; ZHONG N; BROWN WT
      TISSUE DIFFERENCES IN FRAGILE-X MOSAICS - MOSAICISM IN BLOOD-CELLS MAY DIFFER GREATLY FROM SKIN

      American journal of medical genetics
    68. MADDALENA A; YADVISH KN; SPENCE WC; HOWARDPEEBLES PN
      A FRAGILE-X MOSAIC MALE WITH A CRYPTIC FULL MUTATION DETECTED IN EPITHELIUM BUT NOT IN BLOOD

      American journal of medical genetics
    69. SOBESKY WE; TAYLOR AK; PENNINGTON BF; BENNETTO L; PORTER D; RIDDLE J; HAGERMAN RJ
      MOLECULAR CLINICAL CORRELATIONS IN FEMALES WITH FRAGILE-X/

      American journal of medical genetics
    70. WRIGHTTALAMANTE C; CHEEMA A; RIDDLE JE; LUCKEY DW; TAYLOR AK; HAGERMAN RJ
      A CONTROLLED-STUDY OF LONGITUDINAL IQ CHANGES IN FEMALES AND MALES WITH FRAGILE-X SYNDROME

      American journal of medical genetics
    71. MERENSTEIN SA; SOBESKY WE; TAYLOR AK; RIDDLE JE; TRAN HX; HAGERMAN RJ
      MOLECULAR-CLINICAL CORRELATIONS IN MALES WITH AN EXPANDED FMR1 MUTATION

      American journal of medical genetics
    72. HAGERMAN RJ
      BIOMEDICAL ADVANCES IN DEVELOPMENTAL-PSYCHOLOGY - THE CASE OF FRAGILE-X SYNDROME

      Developmental psychology
    73. NOLIN SL; LEWIS FA; YE LL; HOUCK GE; GLICKSMAN AE; LIMPRASERT P; LI SY; ZHONG N; ASHLEY AE; FEINGOLD E; SHERMAN SL; BROWN WT
      FAMILIAL TRANSMISSION OF THE FMR1 CGG REPEAT

      American journal of human genetics
    74. VAISANEN ML; HAATAJA R; LEISTI L
      DECREASE IN THE CGG(N) TRINUCLEOTIDE REPEAT MUTATION OF THE FRAGILE-XSYNDROME TO NORMAL SIZE RANGE DURING PATERNAL TRANSMISSION

      American journal of human genetics
    75. NELSON DL
      THE FRAGILE-X SYNDROMES

      Seminars in cell biology
    76. WOHRLE D; KENNERKNECHT I; WOLF M; ENDERS H; SCHWEMMLE S; STEINBACH P
      HETEROGENEITY OF DM KINASE REPEAT EXPANSION IN DIFFERENT FETAL TISSUES AND FURTHER EXPANSION DURING CELL-PROLIFERATION IN-VITRO - EVIDENCE FOR A CAUSAL INVOLVEMENT OF METHYL-DIRECTED DNA MISMATCH REPAIR IN TRIPLET REPEAT STABILITY

      Human molecular genetics
    77. DREESEN JCFM; GERAEDTS JPM; DUMOULIN JCM; EVERS JLH; PIETERS MHEC
      RS46(DXS548) GENOTYPING OF REPRODUCTIVE CELLS - APPROACHING PREIMPLANTATION TESTING OF THE FRAGILE-X SYNDROME

      Human genetics
    78. MORRIS A; MORTON NE; COLLINS A; MACPHERSON J; NELSON D; SHERMAN S
      AN N-ALLELE MODEL FOR PROGRESSIVE AMPLIFICATION IN THE FMR1 LOCUS

      Proceedings of the National Academy of Sciences of the United Statesof America
    79. BANARES VG
      UPDATING THE FRAGILE-X SYNDROME

      Medicina
    80. LOESCH DZ; HUGGINS R; PETROVIC V; SLATER H
      EXPANSION OF THE CGG REPEAT IN FRAGILE-X IN THE FMR1 GENE DEPENDS ON THE SEX OF THE OFFSPRING

      American journal of human genetics
    81. ASHLEY AE; SHERMAN SL
      POPULATION-DYNAMICS OF A MEIOTIC MITOTIC EXPANSION MODEL FOR THE FRAGILE-X SYNDROME

      American journal of human genetics
    82. DEGRAAFF E; WILLEMSEN R; ZHONG N; DEDIESMULDERS CEM; BROWN WT; FRELING G; OOSTRA B
      INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF THE FMR1 PROTEIN IN AMALE FRAGILE-X PATIENT WITH A LUNG-TUMOR

      American journal of human genetics
    83. FISCH GS; SNOW K; THIBODEAU SN; CHALIFAUX M; HOLDEN JJA; NELSON DL; HOWARDPEEBLES PN; MADDALENA A
      THE FRAGILE-X PREMUTATION IN CARRIERS AND ITS EFFECT ON MUTATION SIZEIN OFFSPRING

      American journal of human genetics
    84. FENG Y; LAKKIS L; DEVYS D; WARREN ST
      QUANTITATIVE COMPARISON OF FMRI GENE-EXPRESSION IN NORMAL AND PREMUTATION ALLELES

      American journal of human genetics
    85. EICHLER EE; HOLDEN JJA; POPOVICH BW; REISS AL; SNOW K; THIBODEAU SN; RICHARDS CS; WARD PA; NELSON DL
      LENGTH OF UNINTERRUPTED CGG REPEATS DETERMINES INSTABILITY IN THE FMR1 GENE

      Nature genetics
    86. ROUSSEAU F; ROBB LJ; ROUILLARD P; DERKALOUSTIAN VM
      NO MENTAL-RETARDATION IN A MAN WITH 40-PERCENT ABNORMAL METHYLATION AT THE FMR-1 LOCUS AND TRANSMISSION OF SPERM CELL MUTATIONS AS PREMUTATIONS

      Human molecular genetics
    87. VANDENOUWELAND AMW; DEELEN WH; KUNST CB; UZIELLI MLG; NELSON DL; WARREN ST; OOSTRA BA; HALLEY DJJ
      LOSS OF MUTATION AT THE FMR1 LOCUS THROUGH MULTIPLE EXCHANGES BETWEENMATERNAL X-CHROMOSOMES

      Human molecular genetics
    88. VITS L; DEBOULLE K; REYNIERS E; HANDIG I; DARBY JK; OOSTRA B; WILLEMS PJ
      APPARENT REGRESSION OF THE CGG REPEAT IN FMR1 TO AN ALLELE OF NORMAL SIZE

      Human genetics
    89. VAISANEN ML; KAHKONEN M; LEISTI J
      DIAGNOSIS OF FRAGILE-X SYNDROME BY DIRECT MUTATION ANALYSIS

      Human genetics
    90. JENKINS EC; MORYS I; HENDERSON J; GENOVESE M; CARTER M; LI SY; HOUCK GE; DING XH; STARKHOUCK SL; DOBKIN CS; BROWN WT
      FRAGILE-X INDUCTION SYSTEMS IN CVS CULTURES - EFFECT ON CYTOGENETIC, PCR, AND GENOMIC SOUTHERN BLOT DNA ANALYSES OF THE FMR-1 GENE

      American journal of medical genetics
    91. VONKOSKULL H; GAHMBERG N; SALONEN R; SALO A; PEIPPO M
      FRAXA LOCUS IN FRAGILE-X DIAGNOSIS - FAMILY STUDIES, PRENATAL-DIAGNOSIS, AND DIAGNOSIS OF SPORADIC CASES OF MENTAL-RETARDATION

      American journal of medical genetics
    92. CHIURAZZI P; KOZAK L; NERI G
      UNSTABLE TRIPLETS AND THEIR MUTATIONAL MECHANISM - SIZE-REDUCTION OF THE CGG REPEAT VS GERMLINE MOSAICISM IN THE FRAGILE-X-SYNDROME

      American journal of medical genetics
    93. LEVINSON G; MADDALENA A; PALMER FT; HARTON GL; BICK DP; HOWARDPEEBLES PN; BLACK SH; SCHULMAN JD
      IMPROVED SIZING OF FRAGILE-X CCG REPEATS BY NESTED POLYMERASE CHAIN-REACTION

      American journal of medical genetics
    94. ROUSSEAU F
      THE FRAGILE-X SYNDROME - IMPLICATIONS OF MOLECULAR-GENETICS FOR THE CLINICAL SYNDROME

      European journal of clinical investigation
    95. ROUSSEAU F; HEITZ D; TARLETON J; MACPHERSON J; MALMGREN H; DAHL N; BARNICOAT A; MATHEW C; MORNET E; TEJADA I; MADDALENA A; SPIEGEL R; SCHINZEL A; MARCOS JAG; SCHORDERET DF; SCHAAP T; MACCIONI L; RUSSO S; JACOBS PA; SCHWARTZ C; MANDEL JL
      A MULTICENTER STUDY ON GENOTYPE-PHENOTYPE CORRELATIONS IN THE FRAGILE-X-SYNDROME, USING DIRECT DIAGNOSIS WITH PROBE STB-12.3 - THE FIRST 2,253 CASES

      American journal of human genetics


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Documento generato il 18/02/20 alle ore 04:59:41