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    1. Chelly, J; Mandel, JL
      Monogenic causes of X-linked mental retardation

      NATURE REVIEWS GENETICS
    2. Mallolas, J; Duran, M; Sanchez, A; Jimenez, D; Castellvi-Bel, S; Rife, M; Mila, M
      Implications of the FMR1 gene in menopause: study of 147 Spanish women

      MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY
    3. 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
    4. Fulmer-Smentek, SB; Francke, U
      Association of acetylated histones with paternally expressed genes in the Prader-Willi deletion region

      HUMAN MOLECULAR GENETICS
    5. Grabczyk, E; Kumari, D; Usdin, K
      Fragile X syndrome and Friedreich's ataxia: Two different paradigms for repeat induced transcript insufficiency

      BRAIN RESEARCH BULLETIN
    6. Chiurazzi, P; Neri, G
      Pharmacological reactivation of inactive genes: The fragile X experience

      BRAIN RESEARCH BULLETIN
    7. Weinhausel, A; Haas, OA
      Evaluation of the fragile X (FRAXA) syndrome with methylation-sensitive PCR

      HUMAN GENETICS
    8. 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
    9. Apessos, A; Abou-Sleiman, PM; Harper, JC; Delhanty, JDA
      Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers

      PRENATAL DIAGNOSIS
    10. 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
    11. Bacolla, A; Pradhan, S; Larson, JE; Roberts, RJ; Wells, RD
      Recombinant human DNA (cytosine-5) methyltransferase - III. Allosteric control, reaction order, and influence of plasmid topology and triplet repeat length on methylation of the fragile X CGG center dot CCG sequence

      JOURNAL OF BIOLOGICAL CHEMISTRY
    12. Wohrle, D; Salat, U; Hameister, H; Vogel, W; Steinbach, P
      Demethylation, reactivation, and destabilization of human fragile X full-mutation alleles in mouse embryocarcinoma cells

      AMERICAN JOURNAL OF HUMAN GENETICS
    13. Toledano-Alhadef, H; Basel-Vanagaite, L; Magal, N; Davidov, B; Ehrlich, S; Drasinover, V; Taub, E; Halpern, GJ; Ginott, N; Shohat, M
      Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel

      AMERICAN JOURNAL OF HUMAN GENETICS
    14. Burman, RW; Anoe, KS; Popovich, BW
      Fragile X full mutations ave more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamics

      GENETICS IN MEDICINE
    15. 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
    16. Mazzocco, MMM
      Advances in research on the fragile X syndrome

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    17. Block, SS; Brusca-Vega, R; Pizzi, WJ; Berry-Kravis, E; Maino, DM; Treitman, TM
      Cognitive and visual processing skills and their relationship to mutation size in full and premutation female fragile X carriers

      OPTOMETRY AND VISION SCIENCE
    18. Gaitskhoki, VS; Patkin, EL
      Satellite DNAs and diseases - Possible mechanisms: Trinucleotide repeats

      RUSSIAN JOURNAL OF GENETICS
    19. Jin, P; Warren, ST
      Understanding the molecular basis of fragile X syndrome

      HUMAN MOLECULAR GENETICS
    20. Crawford, DC; Zhang, FP; Wilson, B; Warren, ST; Sherman, SL
      Fragile X CGG repeat structures among African-Americans: identification ofa novel factor responsible for repeat instability

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

      NEUROSCIENCE RESEARCH COMMUNICATIONS
    22. Mila, M; Castellvi-Bel, S; Sanchez, A; Barcelo, A; Badenas, C; Mallolas, J; Estivill, X
      Rare variants in the promoter of the fragile X syndrome gene (FMR1)

      MOLECULAR AND CELLULAR PROBES
    23. Weisman-Shomer, P; Cohen, E; Fry, M
      Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structures

      NUCLEIC ACIDS RESEARCH
    24. Tariverdian, G; Vogel, F
      Some problems in the genetics of X-linked mental retardation

      CYTOGENETICS AND CELL GENETICS
    25. Marozzi, A; Vegetti, W; Manfredini, E; Tibiletti, MG; Testa, G; Crosignani, PG; Ginelli, E; Meneveri, R; Dalpra, L
      Association between idiopathic premature ovarian failure and fragile X premutation

      HUMAN REPRODUCTION
    26. Willemsen, R; Oostra, BA
      FMRP detection assay for the diagnosis of the fragile X syndrome

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

      AMERICAN JOURNAL OF MEDICAL GENETICS
    28. Backes, M; Genc, B; Schreck, J; Doerfler, W; Lehmkuhl, G; von Gontard, A
      Cognitive and behavioral profile of fragile X boys: Correlations to molecular data

      AMERICAN JOURNAL OF MEDICAL GENETICS
    29. Larsen, LA; Armstrong, JSM; Gronskov, K; Hjalgrim, H; Macpherson, JN; Brondum-Nielsen, K; Hasholt, L; Norgaard-Pedersen, B; Vuust, J
      Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: Implications for multiple mutational pathways towards fragile X alleles

      AMERICAN JOURNAL OF MEDICAL GENETICS
    30. Uliel, L; Weisman-Shomer, P; Oren-Jazans, H; Newcomb, T; Loeb, LA; Fry, M
      Human Ku antigen tightly binds and stabilizes a tetrahelical form of the fragile X syndrome d(CGG)(n) expanded sequence

      JOURNAL OF BIOLOGICAL CHEMISTRY
    31. Kallinen, J; Heinonen, S; Mannermaa, A; Ryynanen, M
      Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation

      CLINICAL GENETICS
    32. Tzeng, CC; Cho, WC; Kuo, PL; Chen, RM
      Pilot fragile X screening in normal population of Taiwan

      DIAGNOSTIC MOLECULAR PATHOLOGY
    33. Larsen, LA; Armstrong, JSM; Gronskov, K; Hjalgrim, H; Brondum-Nielsen, K; Hasholt, L; Norgaard-Pedersen, B; Vuust, J
      Analysis of FMR1 (CGG)(n) alleles and FRAXA microsatellite haplotypes in the population of Greenland: implications for the population of the New World from Asia

      EUROPEAN JOURNAL OF HUMAN GENETICS
    34. Wang, L; Darling, J; Zhang, JS; Huang, HJ; Liu, WG; Smith, DI
      Allele-specific late replication and fragility of the most active common fragile site, FRA3B

      HUMAN MOLECULAR GENETICS
    35. Orlov, SV; Dizhe, EB; Kuteikin, KB; Kuryshev, VY; Perevozchikov, AP
      Functional activity of GCC-element induced in the homologous regulatory region of some mammalian genes

      DOKLADY AKADEMII NAUK
    36. Sun, YJ; Baumer, A
      Nonrandom X inactivation and selection of fragile X full mutation in fetalfibroblasts

      AMERICAN JOURNAL OF MEDICAL GENETICS
    37. Grasso, M; Faravelli, F; Lo Nigro, C; Chiurazzi, P; Sperandeo, MP; Argusti, A; Pomponi, MG; Lecora, M; Sebastio, GF; Perroni, L; Andria, G; Neri, G; Bricarelli, FD
      Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients

      AMERICAN JOURNAL OF MEDICAL GENETICS
    38. Pang, CP; Poon, PMK; Chen, QL; Lai, KYC; Yin, CH; Zhao, Z; Zhong, N; Lau, CH; Lam, STS; Wong, CK; Brown, WT
      Trinucleotide CGG repeat in the FMR1 gene in Chinese mentally retarded patients

      AMERICAN JOURNAL OF MEDICAL GENETICS
    39. Haddad, LA; Aguiar, MJB; Costa, SS; Mingroni-Netto, RC; Vianna-Morgante, AM; Pena, SDJ
      Fully mutated and gray-zone FRAXA alleles in Brazilian mentally retarded boys

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

      AMERICAN JOURNAL OF MEDICAL GENETICS
    41. 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
    42. Castellvi-Bel, S; Sanchez, A; Badenas, C; Mallolas, J; Barcelo, A; Jimenez, D; Villa, M; Estivill, X; Mila, M
      Single-strand conformation polymorphism analysis in the FMR1 gene

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

      AMERICAN JOURNAL OF MEDICAL GENETICS
    44. Neri, G; Chiurazzi, P
      X-linked mental retardation

      ADVANCES IN GENETICS, VOL 41
    45. Orlov, SV; Kuteikin, KB; Dizhe, EB; Kuryshev, VY; Shpakovich, VM; Perevozchikov, AP
      DNA-protein interactions between mammalian nuclear proteins and a GCC-element included in a composite cis-acting element of mouse ribosomal protein L32 promoter

      BIOCHEMISTRY-MOSCOW
    46. Huang, T; Li, LY; Fan, Y; Vicaire, S; Pang, ZL; Mandel, JL; Wu, GY; Shen, Y
      Alternative splicing of FMR1 gene in fetal and adult human brain

      PROGRESS IN NATURAL SCIENCE
    47. ORRICO A; GALLI L; DOTTI MT; PLEWNIA K; CENSINI S; FEDERICO A
      MOSAICISM FOR FULL MUTATION AND NORMAL-SIZED ALLELE OF THE FMR1 GENE - A NEW CASE

      American journal of medical genetics
    48. MURRAY A; WEBB J; GRIMLEY S; CONWAY G; JACOBS P
      STUDIES OF FRAXA AND FRAXE IN WOMEN WITH PREMATURE OVARIAN FAILURE

      Journal of Medical Genetics
    49. DEVRIES BBA; HALLEY DJJ; OOSTRA BA; NIERMEIJER MF
      THE FRAGILE-X-SYNDROME

      Journal of Medical Genetics
    50. RUSSO S; BRISCIOLI V; COGLIATI F; MACCHI M; LALATTA F; LARIZZA L
      AN UNUSUAL FRAGILE-X SIBSHIP - FEMALE COMPOUND HETEROZYGOTE AND MALE WITH A PARTIALLY METHYLATED FULL MUTATION

      Clinical genetics
    51. BONTEKOE CJM; DEGRAAFF E; NIEUWENHUIZEN IM; WILLEMSEN R; OOSTRA BA
      FMR1 PREMUTATION ALLELE (CGG)(81) IS STABLE IN MICE

      European journal of human genetics
    52. MOUTOU C; VINCENT MC; BIANCALANA V; MANDEL JL
      TRANSITION FROM PREMUTATION TO FULL MUTATION IN FRAGILE-X-SYNDROME ISLIKELY TO BE PREZYGOTIC

      Human molecular genetics
    53. MURRAY A; MACPHERSON JN; POUND MC; SHARROCK A; YOUINGS SA; DENNIS NR; MCKECHNIE N; LINEHAN P; MORTON NE; JACOBS PA
      THE ROLE OF SIZE, SEQUENCE AND HAPLOTYPE IN THE STABILITY OF FRAXA AND FRAXE ALLELES DURING TRANSMISSION

      Human molecular genetics
    54. OOSTRA BA; HOOGEVEEN AT
      ANIMAL-MODEL FOR FRAGILE-X-SYNDROME

      Annals of medicine
    55. HOOGEVEEN AT; OOSTRA BA
      THE FRAGILE-X-SYNDROME

      Journal of inherited metabolic disease
    56. HANSEN RS; CANFIELD TK; FJELD AD; MUMM S; LAIRD CD; GARTLER SM
      A VARIABLE DOMAIN OF DELAYED REPLICATION IN FRAXA FRAGILE-X CHROMOSOMES - X INACTIVATION-LIKE SPREAD OF LATE REPLICATION

      Proceedings of the National Academy of Sciences of the United Statesof America
    57. 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
    58. LOSEKOOT M; HOOGENDOORN E; OLMER R; JANSEN CCAM; OOSTERWIJK JC; VANDENOUWELAND AMW; HALLEY DJJ; WARREN ST; WILLEMSEN R; OOSTRA BA; BAKKER E
      PRENATAL-DIAGNOSIS OF THE FRAGILE-X-SYNDROME - LOSS OF MUTATION OWINGTO A DOUBLE RECOMBINANT OR GENE CONVERSION EVENT AT THE FMR1 LOCUS

      Journal of Medical Genetics
    59. SCRABLE H; STAMBROOK PJ
      ACTIVATION OF THE LAC REPRESSOR IN THE TRANSGENIC MOUSE

      Genetics
    60. HECIMOVIC S; BARISIC I; MULLER A; PETKOVIC I; BARIC I; LIGUTIC I; PAVELIC K
      EXPAND LONG PCR FOR FRAGILE-X MUTATION DETECTION

      Clinical genetics
    61. IMBERT G; SAUDOU F; YVERT G; DEVYS D; TROTTIER Y; GARNIER JM; WEBER C; MANDEL JL; CANCEL G; ABBAS N; DURR A; DIDIERJEAN O; STEVANIN G; AGID Y; BRICE A
      CLONING OF THE GENE FOR SPINOCEREBELLAR ATAXIA-2 REVEALS A LOCUS WITHHIGH-SENSITIVITY TO EXPANDED CAG GLUTAMINE REPEATS/

      Nature genetics
    62. EBERHART DE; WARREN ST
      NUCLEASE SENSITIVITY OF PERMEABILIZED CELLS CONFIRMS ALTERED CHROMATIN FORMATION AT THE FRAGILE-X LOCUS

      Somatic cell and molecular genetics
    63. JI JP; CLEGG NJ; PETERSON KR; JACKSON AL; LAIRD CD; LOEB LA
      IN-VITRO EXPANSION OF GGC-GCC REPEATS - IDENTIFICATION OF THE PREFERRED STRAND OF EXPANSION

      Nucleic acids research
    64. PETRONIS A
      GENOMIC IMPRINTING IN UNSTABLE DNA DISEASES

      BioEssays
    65. IBER H
      SEQUENCE-SPECIFIC BINDING OF CYTOSOLIC PROTEINS TO A 12 NUCLEOTIDE-SEQUENCE IN THE 5'-UNTRANSLATED REGION OF FMR1 MESSENGER-RNA

      Biochimica et biophysica acta, N. Gene structure and expression
    66. HUANG T; LI LY; SHEN Y; QIN XB; PANG ZL; WU GY
      ALTERNATIVE SPLICING OF THE FMR1 GENE IN HUMAN FETAL BRAIN NEURONS

      American journal of medical genetics
    67. 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
    68. STEYAERT J; BORGHGRAEF M; LEGIUS E; FRYNS JP
      MOLECULAR-INTELLIGENCE CORRELATIONS IN YOUNG FRAGILE-X MALES WITH A MILD CGG REPEAT EXPANSION IN THE FMR1 GENE

      American journal of medical genetics
    69. STALEYGANE L; FLYNN L; NEITZEL K; CRONISTER A; HAGERMAN RJ
      EXPANDING THE ROLE OF THE GENETIC COUNSELOR

      American journal of medical genetics
    70. 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
    71. REYNIERS E; WOLFF G; TARIVERDIAN G; DEBOULLE K; STORM K; KOOY RF; WILLEMS PJ
      SEVERE MENTAL-RETARDATION AND MACROORCHIDISM WITHOUT MUTATION IN THE FMR1 GENE

      American journal of medical genetics
    72. HOLDEN JJA; WALKER M; CHALIFOUX M; WHITE BN
      TRINUCLEOTIDE REPEATS AT THE FRAXF LOCUS - FREQUENCY AND DISTRIBUTIONIN THE GENERAL-POPULATION

      American journal of medical genetics
    73. WANG ZM; TAYLOR AK; BRIDGE JA
      FMR1 FULLY EXPANDED MUTATION WITH MINIMAL METHYLATION IN A HIGH-FUNCTIONING FRAGILE-X MALE

      Journal of Medical Genetics
    74. MILA M; CASTELLVIBEL S; SANCHEZ A; LAZARO C; VILLA M; ESTIVILL X
      MOSAICISM FOR THE FRAGILE-X SYNDROME FULL MUTATION AND DELETIONS WITHIN THE CGG REPEAT OF THE FMR1 GENE

      Journal of Medical Genetics
    75. PEARSON CE; SINDEN RR
      ALTERNATIVE STRUCTURES IN DUPLEX DNA FORMED WITHIN THE TRINUCLEOTIDE REPEATS OF THE MYOTONIC-DYSTROPHY AND FRAGILE-X LOCI

      Biochemistry
    76. 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
    77. SUBRAMANIAN PS; NELSON DL; CHINAULT AC
      LARGE DOMAINS OF APPARENT DELAYED REPLICATION TIMING ASSOCIATED WITH TRIPLET REPEAT EXPANSION AT FRAXA AND FRAXE

      American journal of human genetics
    78. MILEWSKI M; ZYGULSKA M; BAL J; DEELEN WH; OBERSZTYN E; BOCIAN E; HALLEY DJJ; HORST J; MAZURCZAK T
      ANALYSIS OF UNSTABLE DNA-SEQUENCE IN FRM1 GENE IN POLISH FAMILIES WITH FRAGILE-X SYNDROME

      Acta Biochimica Polonica
    79. FLANNERY AV; HIRST MC; KNIGHT SJL; RITCHIE RJ; DAVIES KE
      THE FRAGILE-X SYNDROME

      Biochimica et biophysica acta. Molecular basis of disease
    80. DOMINGUEZ AM; SMITH SA; GREENBAUM IF
      SUSCEPTIBILITY OF HETEROCHROMATIN TO APHIDICOLIN-INDUCED CHROMOSOMAL BREAKAGE

      Human genetics
    81. OOSTRA BA; WILLEMS PJ
      A FRAGILE GENE

      BioEssays
    82. WARREN ST; ASHLEY CT
      TRIPLET REPEAT EXPANSION MUTATIONS - THE EXAMPLE OF FRAGILE-X SYNDROME

      Annual review of neuroscience
    83. ASHLEY CT; WARREN ST
      TRINUCLEOTIDE REPEAT EXPANSION AND HUMAN-DISEASE

      Annual review of genetics
    84. OOSTRA BA; HALLEY DJJ
      COMPLEX BEHAVIOR OF SIMPLE REPEATS - THE FRAGILE-X SYNDROME

      Pediatric research
    85. NADEL Y; WEISMANSHOMER P; FRY M
      THE FRAGILE-X SYNDROME SINGLE-STRAND D(CGG)(N) NUCLEOTIDE REPEATS READILY FOLD BACK TO FORM UNIMOLECULAR HAIRPIN STRUCTURES

      The Journal of biological chemistry
    86. RITCHIE RJ; KNIGHT SJL; HIRST MC; GREWAL PK; BOBROW M; CROSS GS; DAVIES KE
      THE CLONING OF FRAXF - TRINUCLEOTIDE REPEAT EXPANSION AND METHYLATIONAT A 3RD FRAGILE SITE IN DISTAL XQTER

      Human molecular genetics
    87. WILKE CM; GUO SW; HALL BK; BOLDOG F; GEMMILL RM; CHANDRASEKHARAPPA SC; BARCROFT CI; DRABKIN HA; GLOVER TW
      MULTICOLOR FISH MAPPING OF YAC CLONES IN 3P14 AND IDENTIFICATION OF AYAC SPANNING BOTH FRA3B AND THE T(38) ASSOCIATED WITH HEREDITARY RENAL-CELL CARCINOMA

      Genomics
    88. SCHWARTZ CE; DEAN J; HOWARDPEEBLES PN; BUGGE M; MIKKELSEN M; TOMMERUP N; HULL C; HAGERMAN R; HOLDEN JJA; STEVENSON RE
      OBSTETRICAL AND GYNECOLOGICAL COMPLICATIONS IN FRAGILE-X CARRIERS - AMULTICENTER STUDY

      American journal of medical genetics
    89. TROTTIER Y; IMBERT G; POUSTKA A; FRYNS JP; MANDEL JL
      MALE WITH TYPICAL FRAGILE-X PHENOTYPE IS DELETED FOR PART OF THE FMR1GENE AND FOR ABOUT 100 KB OF UPSTREAM REGION

      American journal of medical genetics
    90. SHERMAN SL; MADDALENA A; HOWARDPEEBLES PN; BROWN WT; NOLIN S; JENKINS E; SCHWARTZ C; TARRELTON J; SHAPIRO LR; SMITS APT; VANOOST BA; YOUINGS S; JACOBS PA; MARTINEZ F; BARNICOAT A; HOCKEY A; STALEY L; HAGERMAN R; KENNERKNECHT I; STEINBACH P; BARBI G; FILIPPI G; GRASSO M; TAYLOR SAM; ROBINSON H; WEBB T; BROOME D; DIXON J; FERREIRA P; GUSTAVSON KH; MEYER JL; PAI GS
      CHARACTERISTICS OF THE TRANSMISSION OF THE FMR1 GENE FROM CARRIER FEMALES IN A PROSPECTIVE SAMPLE OF CONCEPTUSES

      American journal of medical genetics
    91. NANCARROW JK; KREMER E; HOLMAN K; EYRE H; DOGGETT NA; LEPASLIER D; CALLEN DF; SUTHERLAND GR; RICHARDS RI
      IMPLICATIONS OF FRA16A STRUCTURE FOR THE MECHANISM OF CHROMOSOMAL FRAGILE SITE GENESIS

      Science
    92. BOGGS BA; CHINAULT C
      ANALYSIS OF REPLICATION TIMING PROPERTIES OF HUMAN X-CHROMOSOMAL LOCIBY FLUORESCENCE IN-SITU HYBRIDIZATION

      Proceedings of the National Academy of Sciences of the United Statesof America
    93. FRY M; LOEB LA
      THE FRAGILE-X SYNDROME D(CGG)(N) NUCLEOTIDE REPEATS FORM A STABLE TETRAHELICAL STRUCTURE

      Proceedings of the National Academy of Sciences of the United Statesof America
    94. LAIRD CD; HANSEN RS; CANFIELD TK; LAMB MM; GARTLER SM
      CHROMOSOMAL FRAGILE SITES - MOLECULAR TEST OF THE DELAYED-REPLICATIONMODEL

      Cold Spring Harbor Symposia on Quantitative Biology


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Documento generato il 07/06/20 alle ore 09:19:08