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

      SEMINARS IN REPRODUCTIVE MEDICINE
    2. Chelly, J; Mandel, JL
      Monogenic causes of X-linked mental retardation

      NATURE REVIEWS GENETICS
    3. Crawford, DC; Acuna, JM; Sherman, SL
      FMR1 and the fragile X syndrome: Human genome epidemiology review

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

      MOLECULAR GENETICS AND METABOLISM
    5. 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
    6. Ennis, S; Murray, A; Morton, NE
      Haplotypic determinants of instability in the FRAX region: Concatenated mutation or founder effect?

      HUMAN MUTATION
    7. Collins, A; Ennis, S; Taillon-Miller, P; Kwok, PY; Morton, NE
      Allelic association with SNPs: Metrics, populations, and the linkage disequilibrium map

      HUMAN MUTATION
    8. 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
    9. Larsen, LA; Vuust, J; Nystad, M; Evseeva, I; Van Ghelue, M; Tranebjaerg, L
      Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia

      EUROPEAN JOURNAL OF HUMAN GENETICS
    10. Kwon, SH; Lee, KS; Hyun, MC; Song, KE; Kim, JK
      Molecular screening for Fragile X syndrome in mentally handicapped children in Korea

      JOURNAL OF KOREAN MEDICAL SCIENCE
    11. Fulmer-Smentek, SB; Francke, U
      Association of acetylated histones with paternally expressed genes in the Prader-Willi deletion region

      HUMAN MOLECULAR GENETICS
    12. Laggerbauer, B; Ostareck, D; Keidel, EM; Ostareck-Lederer, A; Fischer, U
      Evidence that fragile X mental retardation protein is a negative regulatorof translation

      HUMAN MOLECULAR GENETICS
    13. Jun, L; Frints, S; Duhamel, H; Herold, A; Abad-Rodrigues, J; Dotti, C; Izaurralde, E; Marynen, P; Froyen, G
      NXF5, a novel member of the nuclear RNA export factor family, is lost in amale patient with a syndromic form of mental retardation

      CURRENT BIOLOGY
    14. Eliez, S; Feinstein, C
      The fragile X syndrome: bridging the gap from gene to behavior

      CURRENT OPINION IN PSYCHIATRY
    15. Grabczyk, E; Kumari, D; Usdin, K
      Fragile X syndrome and Friedreich's ataxia: Two different paradigms for repeat induced transcript insufficiency

      BRAIN RESEARCH BULLETIN
    16. Bardoni, B; Schenck, A; Mandel, JL
      The Fragile X mental retardation protein

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

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

      HUMAN GENETICS
    19. Li, ZZ; Zhang, YY; Ku, L; Wilkinson, KD; Warren, ST; Feng, Y
      The fragile X mental retardation protein inhibits translation via interacting with mRNA

      NUCLEIC ACIDS RESEARCH
    20. McDowell, JE; Clementz, BA
      Behavioral and brain imaging studies of saccadic performance in schizophrenia

      BIOLOGICAL PSYCHOLOGY
    21. Castren, M; Haapasalo, A; Oostra, BA; Castren, E
      Subcellular localization of fragile X mental retardation protein with the I304N mutation in the RNA-binding domain in cultured hippocampal neurons

      CELLULAR AND MOLECULAR NEUROBIOLOGY
    22. 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
    23. Schaeffer, C; Bardoni, B; Mandel, JL; Ehresmann, B; Ehresmann, C; Moine, H
      The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif

      EMBO JOURNAL
    24. 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
    25. Bailey, DB; Hatton, DD; Skinner, M; Mesibov, G
      Autistic behavior, FMR1 protein, and developmental trajectories in young males with fragile X syndrome

      JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
    26. Limprasert, P; Saechan, V; Ruangdaraganon, N; Sura, T; Vasiknanote, P; Jaruratanasirikul, S; Brown, WT
      Haplotype analysis at the FRAXA locus in Thai subjects

      AMERICAN JOURNAL OF MEDICAL GENETICS
    27. 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
    28. Sun, HT; Cohen, S; Kaufmann, WE
      Annexin-1 is abnormally expressed in fragile X syndrome: Two-dimensional electrophoresis study in lymphocytes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    29. Kaytor, MD; Orr, HT
      RNA targets of the fragile X protein

      CELL
    30. Darnell, JC; Jensen, KB; Jin, P; Brown, V; Warren, ST; Darnell, RB
      Fragile X mental retardation protein targets G quartet mRNAs important forneuronal function

      CELL
    31. McIlwain, KL; Merriweather, MY; Yuva-Paylor, LA; Paylor, R
      The use of behavioral test batteries: Effects of training history

      PHYSIOLOGY & BEHAVIOR
    32. Hessl, D; Dyer-Friedman, J; Glaser, B; Wisbeck, J; Barajas, RG; Taylor, A; Reiss, AL
      The influence of environmental and genetic factors on behavior problems and autistic symptoms in boys and girls with fragile X syndrome

      PEDIATRICS
    33. 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
    34. Eliez, S; Blasey, CM; Freund, LS; Hastie, T; Reiss, AL
      Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome

      BRAIN
    35. 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
    36. 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
    37. Murray, A
      Premature ovarian failure and the FMR1 gene

      SEMINARS IN REPRODUCTIVE MEDICINE
    38. Poon, PMK; Zhao, Z; Wu, XQ; Ni, YX; Pang, CP
      Rapid analysis of CGG repeat length in the FMR1 gene

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    39. Musumeci, SA; Scuderi, C; Ferri, R; Anello, G; Salluzzo, R; Bosco, P; Elia, M
      Does a peculiar EEG pattern exist also for FRAXE mental retardation?

      CLINICAL NEUROPHYSIOLOGY
    40. Kooy, RF; Willemsen, R; Oostra, BA
      Fragile X syndrome at the turn of the century

      MOLECULAR MEDICINE TODAY
    41. Mulatinho, MV; Llerena, JC; Pimentel, MMG
      FRAXE mutation in mentally retarded patients using the OxE18 probe

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    42. 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
    43. 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
    44. Mazzocco, MMM
      Advances in research on the fragile X syndrome

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    45. Irwin, SA; Swain, RA; Christmon, CA; Chakravarti, A; Weiler, IJ; Greenough, WT
      Evidence for altered fragile-x mental retardation protein expression in response to behavioral stimulation (vol 73, pg 87, 2000)

      NEUROBIOLOGY OF LEARNING AND MEMORY
    46. Irwin, SA; Swain, RA; Christmon, CA; Chakravarti, A; Weiler, IJ; Greenough, WT
      Evidence for altered Fragile-X mental retardation protein expression in response to behavioral stimulation

      NEUROBIOLOGY OF LEARNING AND MEMORY
    47. 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
    48. Irwin, SA; Galvez, R; Greenough, WT
      Dendritic spine structural anomalies in fragile-X mental retardation syndrome

      CEREBRAL CORTEX
    49. 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
    50. Gaitskhoki, VS; Patkin, EL
      Satellite DNAs and diseases - Possible mechanisms: Trinucleotide repeats

      RUSSIAN JOURNAL OF GENETICS
    51. Chen, YT; Bardoni, B; Yu, M; Zhu, N; Wu, GY; Mandel, JL; Shen, Y
      Fragile X mental retardation protein interacts with TDG

      CHINESE SCIENCE BULLETIN
    52. Jin, P; Warren, ST
      Understanding the molecular basis of fragile X syndrome

      HUMAN MOLECULAR GENETICS
    53. 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
    54. Tamanini, F; Kirkpatrick, LL; Schonkeren, J; van Unen, L; Bontekoe, C; Bakker, C; Nelson, DL; Galjaard, H; Oostra, BA; Hoogeveen, AT
      The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins

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

      NEUROSCIENCE RESEARCH COMMUNICATIONS
    56. 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
    57. Alakurtti, K; Virtaneva, K; Joensuu, T; Palvimo, JJ; Lehesjoki, AE
      Characterization of the cystatin B gene promoter harboring the dodecamer repeat expanded in progressive myoclonus epilepsy, EPM1

      GENE
    58. Arocena, DG; de Diego, Y; Oostra, BA; Willemsen, R; Rodriguez, MM
      A fragile X case with an amplification/deletion mosaic pattern

      HUMAN GENETICS
    59. 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
    60. 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
    61. Tariverdian, G; Vogel, F
      Some problems in the genetics of X-linked mental retardation

      CYTOGENETICS AND CELL GENETICS
    62. 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
    63. Willemsen, R; Oostra, BA
      FMRP detection assay for the diagnosis of the fragile X syndrome

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

      AMERICAN JOURNAL OF MEDICAL GENETICS
    65. Tuncbilek, E; Alikasifoglu, M; Aktas, D; Duman, F; Yanik, H; Anar, B; Oostra, B; Willemsen, R
      Screening for the fragile X syndrome among mentally retarded males by hairroot analysis

      AMERICAN JOURNAL OF MEDICAL GENETICS
    66. 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
    67. Fryns, JP; Borghgraef, M; Brown, TW; Chelly, J; Fisch, GS; Hamel, B; Hanauer, A; Lacombe, D; Luo, L; MacPherson, JN; Mandel, JL; Moraine, C; Mulley, J; Nelson, D; Oostra, B; Partington, M; Ramakers, GJA; Ropers, HH; Rousseau, F; Schwartz, C; Steinbach, P; Stoll, C; Tranebjaerg, L; Turner, G; Van Bokhoven, H; Vianna-Morgante, A; Villard, L; Warren, ST
      9th international workshop on fragile X syndrome and X-linked mental retardation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    68. 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
    69. 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
    70. Musumeci, SA; Bosco, P; Calabrese, G; Bakker, C; De Sarro, GB; Elia, M; Ferri, R; Oostra, BA
      Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome

      EPILEPSIA
    71. Kallinen, J; Heinonen, S; Mannermaa, A; Ryynanen, M
      Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation

      CLINICAL GENETICS
    72. Ceman, S; Nelson, R; Warren, ST
      Identification of mouse YB1/p50 as a component of the FMRP-associated mRNPparticle

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    73. Saitoh, S; Wada, T
      Parent-of-origin specific histone acetylation and reactivation of a key imprinted gene locus in Prader-Willi syndrome

      AMERICAN JOURNAL OF HUMAN GENETICS
    74. Hundscheid, RDL; Sistermans, EA; Thomas, CMG; Braat, DDM; Straatman, H; Kiemeney, LALM; Oostra, BA; Smits, APT
      Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations

      AMERICAN JOURNAL OF HUMAN GENETICS
    75. Crawford, DC; Schwartz, CE; Meadows, KL; Newman, JL; Taft, LF; Gunter, C; Brown, WT; Carpenter, NJ; Howard-Peebles, PN; Monaghan, KG; Nolin, SL; Reiss, AL; Feldman, GL; Rohlfs, EM; Warren, ST; Sherman, SL
      Survey of the fragile X syndrome CGG repeat and the short-tendem-repeat and single-nucleotide-polymorphism haplotypes in an African American population

      AMERICAN JOURNAL OF HUMAN GENETICS
    76. Adinolfi, S; Bagni, C; Musco, G; Gibson, T; Mazzarella, L; Pastore, A
      Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains

      RNA-A PUBLICATION OF THE RNA SOCIETY
    77. Pimentel, MMG
      Fragile X syndrome

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    78. Tzeng, CC; Cho, WC; Kuo, PL; Chen, RM
      Pilot fragile X screening in normal population of Taiwan

      DIAGNOSTIC MOLECULAR PATHOLOGY
    79. 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
    80. Kan, D; Li, LY; Fan, Y; Xu, Q; Han, FT; Zhu, NN; Liu, EL; Lin, BC; Wu, GY; Shen, Y
      Alternative splicing of the FMR1 gene in human tissues of fetal and adult

      PROGRESS IN NATURAL SCIENCE
    81. Lewis, HA; Chen, H; Edo, C; Buckanovich, RJ; Yang, YYL; Musunuru, K; Zhong, R; Darnell, RB; Burley, SK
      Crystal structures of Nova-1 and Nova-2 K-homology RNA-binding domains

      STRUCTURE WITH FOLDING & DESIGN
    82. 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
    83. Harris, SW; Hagerman, RJ
      Fragile X syndrome: new developments

      CURRENT OPINION IN PSYCHIATRY
    84. Fraternali, F; Amodeo, P; Musco, G; Nilges, M; Pastore, A
      Exploring protein interiors: The role of a buried histidine in the KH module fold

      PROTEINS-STRUCTURE FUNCTION AND GENETICS
    85. 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
    86. Khandjian, EW
      Biology of the fragile X mental retardation protein, an RNA-binding protein

      BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE
    87. Liu, YJ; Pu, YL; Fox, PT; Gao, JH
      Quantification of dynamic changes in cerebral venous oxygenation with MR phase imaging at 1.9 T

      MAGNETIC RESONANCE IN MEDICINE
    88. Bhatia, R; Dube, DK; Gaur, A; Robertson, DR; Lemanski, SL; McLean, MD; Lemanski, LF
      Expression of axolotl RNA-binding protein during development of the Mexican axolotl

      CELL AND TISSUE RESEARCH
    89. Davison, RM; Davis, CJ; Conway, GS
      The X chromosome and ovarian failure

      CLINICAL ENDOCRINOLOGY
    90. Sun, YJ; Baumer, A
      Nonrandom X inactivation and selection of fragile X full mutation in fetalfibroblasts

      AMERICAN JOURNAL OF MEDICAL GENETICS
    91. 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
    92. 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
    93. 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
    94. Mingroni-Netto, RC; Costa, SS; Angeli, CB; Vianna-Morgante, AM
      DXS548/FRAXAC1 haplotypes in fragile X chromosomes in the Brazilian population

      AMERICAN JOURNAL OF MEDICAL GENETICS
    95. Poon, PMK; Pang, CP; Chen, QL; Zhong, N; Lai, KYC; Lau, CH; Wong, CK; Brown, WT
      FRAXAC1 and DXS548 polymorphisms in the Chinese population

      AMERICAN JOURNAL OF MEDICAL GENETICS
    96. Patsalis, PC; Sismani, C; Stylianou, S; Ioannou, P; Joseph, G; Manoli, P; Holden, JJA; Hettinger, JA
      Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population

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

      AMERICAN JOURNAL OF MEDICAL GENETICS
    98. 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
    99. 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
    100. Reyniers, E; Martin, JJ; Cras, P; Van Marck, E; Handig, I; Jorens, HZJ; Oostra, BA; Kooy, RF; Willems, PJ
      Postmortem examination of two fragile X brothers with an FMR1 full mutation

      AMERICAN JOURNAL OF MEDICAL GENETICS


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Documento generato il 20/02/20 alle ore 03:59:27