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

      SEMINARS IN REPRODUCTIVE MEDICINE
    2. Lin, CH; Tsai, SJ; Yu, YWY; Yang, KW; Hsu, CP; Hong, CJ
      Study of anticipation in Chinese families with schizophrenia

      PSYCHIATRY AND CLINICAL NEUROSCIENCES
    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. Gilbert, F
      Comment: How many are too many when discussing triplet repeats in the FMR1gene and the fragile X syndrome?

      GENETIC TESTING
    6. 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
    7. 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
    8. 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
    9. Cornish, KM; Munir, F; Cross, G
      Differential impact of the FMR-1 full mutation on memory and attention functioning: A neuropsychological perspective

      JOURNAL OF COGNITIVE NEUROSCIENCE
    10. Sharma, D; Gupta, M; Thelma, BK
      Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population

      GENETIC EPIDEMIOLOGY
    11. Grabczyk, E; Kumari, D; Usdin, K
      Fragile X syndrome and Friedreich's ataxia: Two different paradigms for repeat induced transcript insufficiency

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

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

      BRAIN RESEARCH BULLETIN
    14. Holmes, SE; O'Hearn, E; Ross, CA; Margolis, RL
      SCA12: An unusual mutation leads to an unusual spinocerebellar ataxia

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

      HUMAN GENETICS
    16. Bacon, AL; Dunlop, MG; Farrington, SM
      Hypermutability at a poly(A/T) tract in the human germline

      NUCLEIC ACIDS RESEARCH
    17. Angers, M; Cloutier, JF; Castonguay, A; Drouin, R
      Optimal conditions to use Pfu exo(-) DNA polymerase for highly efficient ligation-mediated polymerase chain reaction protocols

      NUCLEIC ACIDS RESEARCH
    18. 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
    19. 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
    20. Schultz-Pedersen, S; Hasle, H; Olsen, JH; Friedrich, U
      Evidence of decreased risk of cancer in individuals with fragile X

      AMERICAN JOURNAL OF MEDICAL GENETICS
    21. Zhang, YQ; Bailey, AM; Matthies, HJG; Renden, RB; Smith, MA; Speese, SD; Rubin, GM; Broadie, K
      Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function

      CELL
    22. 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
    23. Chiang, PW; Carpenter, LE; Hagerman, PJ
      The 5 '-untranslated region of the FMR1 message facilitates translation byinternal ribosome entry

      JOURNAL OF BIOLOGICAL CHEMISTRY
    24. Saha, S; Karmakar, P; Chatterjee, C; Banerjee, D; Das, S; Dasgupta, UB
      Fragile X syndrome in Calcutta, India

      ANNALS OF CLINICAL BIOCHEMISTRY
    25. Faradz, SMH; Leggo, J; Murray, A; Lam-Po-Tang, PRL; Buckley, MF; Holden, JJA
      Distribution of FMR1 and FMR2 alleles in Javanese individuals with developmental disability and confirmation of a specific AGG-interruption pattern in Asian populations

      ANNALS OF HUMAN GENETICS
    26. 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
    27. 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
    28. 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
    29. Mulatinho, MV; Llerena, JC; Pimentel, MMG
      FRAXA screening in Brazilian institutionalized individuals with nonspecific severe mental retardation

      GENETIC TESTING
    30. Geva, E; Yaron, Y; Shomrat, R; Ben-Yehuda, A; Zabari, S; Peretz, H; Naiman, T; Yeger, H; Orr-Urtreger, A
      The risk of Fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known Fragile X families

      GENETIC TESTING
    31. 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
    32. Francis, D; Burgess, T; Mitchell, J; Slater, H
      Identification of small FRAXA premutations

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

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    34. 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
    35. Kaushik, N; Malaspina, A; de Belleroche, J
      Characterization of trinucleotide- and tandem repeat-containing transcripts obtained from human spinal cord cDNA library by high-density filter hybridization

      DNA AND CELL BIOLOGY
    36. 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
    37. Murray, A; Ennis, S; Youings, SA; Sharrock, AJ; Lewis, C; Pound, MC; Macpherson, JN; Dennis, NR; Morton, NE; Jacobs, PA
      Stability and haplotype analysis of the FRAXE region

      EUROPEAN JOURNAL OF HUMAN GENETICS
    38. Peier, AM; McIlwain, KL; Kenneson, A; Warren, ST; Paylor, R; Nelson, DL
      (Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical features

      HUMAN MOLECULAR GENETICS
    39. Jones, C; Mullenbach, R; Grossfeld, P; Auer, R; Favier, R; Chien, K; James, M; Tunnacliffe, A; Cotter, F
      Co-localisation of CCG repeats and chromosome deletion breakpoints in Jacobsen syndrome: evidence for a common mechanism of chromosome breakage

      HUMAN MOLECULAR GENETICS
    40. Wang, YC; Li, C; Lin, ML; Lin, WH; Li, SY
      Molecular diagnosis of fragile X syndrome and distribution of CGG repeats in the FMR-1 gene in Taiwanese

      JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
    41. de Vries, BBA; Oostra, BA
      The fragile X syndrome: A model for mental retardation

      NEUROSCIENCE RESEARCH COMMUNICATIONS
    42. Bakker, CE; Kooy, RF; D'Hooge, R; Tamanini, F; Willemsen, R; Nieuwenhuizen, I; De Vries, BBA; Reyniers, E; Hoogeveen, AT; Willems, PJ; De Deyn, PP; Oostra, BA
      Introduction of a FMR1 transgene in the fragile X knockout mouse.

      NEUROSCIENCE RESEARCH COMMUNICATIONS
    43. Granel, B; Ravix, V; Pedeillier, K; Serratrice, J; Disdier, P; Voelckel, MA; Mattei, JF; Weiller, PJ
      A first molecular approach towards CGG repeat expansion in FMR1 gene in systemic lupus erythematosus and in Sjogren's syndrome: A preliminary report

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

      HUMAN GENETICS
    45. Dobkin, C; Rabe, A; Dumas, R; El Idrissi, A; Haubenstock, H; Brown, WT
      Fmr1 knockout mouse has a distinctive strain-specific learning impairment

      NEUROSCIENCE
    46. 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
    47. 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
    48. Tariverdian, G; Vogel, F
      Some problems in the genetics of X-linked mental retardation

      CYTOGENETICS AND CELL GENETICS
    49. Wan, LL; Dockendorff, TC; Jongens, TA; Dreyfuss, G
      Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein

      MOLECULAR AND CELLULAR BIOLOGY
    50. Iqbal, MA; Sakati, N; Nester, M; Ozand, P
      Cytogenetic diagnosis of fragile X syndrome: Study of 305 suspected cases in Saudi Arabia

      ANNALS OF SAUDI MEDICINE
    51. Willemsen, R; Oostra, BA
      FMRP detection assay for the diagnosis of the fragile X syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    52. Tassone, F; Hagerman, RJ; Chamberlain, WD; Hagerman, PJ
      Transcription of the FMR1 gene in individuals with fragile X syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    53. 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
    54. Tassone, F; Hagerman, RJ; Loesch, DZ; Lachiewicz, A; Taylor, AK; Hagerman, PJ
      Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA

      AMERICAN JOURNAL OF MEDICAL GENETICS
    55. 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
    56. 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
    57. Lewis, HA; Musunuru, K; Jensen, KB; Edo, C; Chen, H; Darnell, RB; Burley, SK
      Sequence-specific RNA binding by a Nova KH domain: Implications for paraneoplastic disease and the fragile X syndrome

      CELL
    58. Youings, SA; Murray, A; Dennis, N; Ennis, S; Lewis, C; McKechnie, N; Pound, M; Sharrock, A; Jacobs, P
      FRAXA and FRAXE: the results of a five year survey

      JOURNAL OF MEDICAL GENETICS
    59. Salat, U; Bardoni, B; Wohrle, D; Steinbach, P
      Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: aclue to the sex bias in the transmission of full mutations?

      JOURNAL OF MEDICAL GENETICS
    60. Beresford, RG; Tatlidil, C; Riddell, DC; Welch, JP; Ludman, MD; Neumann, PE; Greer, WL
      Absence of fragile X syndrome in Nova Scotia

      JOURNAL OF MEDICAL GENETICS
    61. Bakker, CE; Otero, YD; Bontekoe, C; Raghoe, P; Luteijn, T; Hoogeveen, AT; Oostra, BA; Willemsen, R
      Immunocytochemical and biochemical characterization of FMRP, FXR1P, and FXR2P in the mouse

      EXPERIMENTAL CELL RESEARCH
    62. 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
    63. Kallinen, J; Heinonen, S; Mannermaa, A; Ryynanen, M
      Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation

      CLINICAL GENETICS
    64. Faradz, SMH; Pattiiha, MZ; Leigh, DA; Jenkins, M; Leggo, J; Buckley, MF; Holden, JJA
      Genetic diversity at the FMR1 locus in the Indonesian population

      ANNALS OF HUMAN GENETICS
    65. Gecz, J
      The FMR2 gene, FRAXE and non-specific X-linked mental retardation: clinical and molecular aspects

      ANNALS OF HUMAN GENETICS
    66. Gonzalez-del Angel, A; Vidal, S; Saldana, Y; del Castillo, V; Alcantara, MA; Macias, M; Luna, JP; Orozco, L
      Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico

      ANNALES DE GENETIQUE
    67. Tassone, F; Hagerman, RJ; Taylor, AK; Gane, LW; Godfrey, TE; Hagerman, PJ
      Elevated levels of FMR1 mRNA in carrier males: A new mechanism of involvement in the fragile-X syndrome

      AMERICAN JOURNAL OF HUMAN GENETICS
    68. Pimentel, MMG
      Fragile X syndrome

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    69. Panagopoulos, I; Lassen, C; Kristoffersson, U; Aman, P
      A methylation PCR approach for detection of fragile X syndrome

      HUMAN MUTATION
    70. Strelnikov, V; Nemtsova, M; Chesnokova, G; Kuleshov, N; Zaletayev, D
      A simple multiplex FRAXA, FRAXE, and FRAXF PCR assay convenient for wide screening programs

      HUMAN MUTATION
    71. Tzeng, CC; Cho, WC; Kuo, PL; Chen, RM
      Pilot fragile X screening in normal population of Taiwan

      DIAGNOSTIC MOLECULAR PATHOLOGY
    72. 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
    73. Wildhagen, MF; van Os, TAM; Polder, JJ; ten Kate, LP; Habbema, JDF
      Efficacy of cascade testing for fragile X syndrome

      JOURNAL OF MEDICAL SCREENING
    74. Bardoni, B; Schenck, A; Mandel, JL
      A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein

      HUMAN MOLECULAR GENETICS
    75. Kirkpatrick, LL; McIlwain, KA; Nelson, DL
      Alternative splicing in the murine and human FXR1 genes

      GENOMICS
    76. Khandjian, EW
      Biology of the fragile X mental retardation protein, an RNA-binding protein

      BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE
    77. Yeshaya, J; Shalgi, R; Shohat, M; Avivi, L
      FISH-detected delay in replication timing of mutated FMR1 alleles on both active and inactive X-chromosomes

      HUMAN GENETICS
    78. Carrillo, C; Cisneros, B; Montanez, C
      Sp1 and AP2 transcription factors are required for the human fragile mental retardation promoter activity in SK-N-SH neuronal cells

      NEUROSCIENCE LETTERS
    79. Kaufmann, WE; Reiss, AL
      Molecular and cellular genetics of fragile X syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    80. Zhong, N; Ju, WN; Xu, WM; Ye, LL; Shen, Y; Wu, GY; Chen, SH; Jin, RM; Hu, XF; Yang, AD; Liu, XX; Poon, P; Pang, C; Zheng, Y; Song, L; Zhao, P; Fu, BJ; Gu, HJ; Brown, WT
      Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians

      AMERICAN JOURNAL OF MEDICAL GENETICS
    81. 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
    82. 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
    83. 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
    84. Schmucker, B; Seidel, J
      Mosaicism for a full mutation and a normal size allele in two fragile X males

      AMERICAN JOURNAL OF MEDICAL GENETICS
    85. 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
    86. 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
    87. 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
    88. 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
    89. 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
    90. Zhong, N; Ju, W; Nelson, D; Dobkin, C; Brown, WT
      Reduced mRNA for G3BP in fragile X cells: Evidence of FMR1 gene regulation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    91. Limprasert, P; Zhong, N; Currie, JR; Brown, WT
      Possible founder effects for FRAXE alleles

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

      AMERICAN JOURNAL OF MEDICAL GENETICS
    93. Parvari, R; Mumm, S; Galil, A; Manor, E; Bar-David, Y; Carmi, R
      Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowth

      AMERICAN JOURNAL OF MEDICAL GENETICS
    94. Dobkin, C; Ding, XH; Li, SY; Houck, G; Nolin, SL; Glicksman, A; Zhong, N; Jenkins, EC; Brown, WT
      Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection

      AMERICAN JOURNAL OF MEDICAL GENETICS
    95. 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
    96. Neri, G; Chiurazzi, P
      X-linked mental retardation

      ADVANCES IN GENETICS, VOL 41
    97. Strelnikov, VV; Nemtsova, MV; Chesnokova, GG; Kuleshov, NP; Zaletaev, DV
      Diagnosis of the Martin-Bell syndrome based on structural and functional alterations in the 5 '-untranslated region of the FMR1 gene

      MOLECULAR BIOLOGY
    98. Agulhon, C; Blanchet, P; Kobetz, A; Marchant, D; Faucon, N; Sarda, P; Moraine, C; Sittler, A; Biancalana, V; Malafosse, A; Abitbol, M
      Expression of FMR1, FXR1, and FXR2 genes in human prenatal tissues

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    99. de Vries, BBA; Mohkamsing, S; van den Ouweland, AMW; Mol, E; Gelsema, K; van Rijn, M; Tibben, A; Halley, DJJ; Duivenvoorden, HJ; Oostra, BA; Niermeijer, MF
      Screening for the fragile X syndrome among the mentally retarded: a clinical study

      JOURNAL OF MEDICAL GENETICS
    100. 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


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Documento generato il 26/05/20 alle ore 20:40:30