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La ricerca find articoli where soggetti phrase all words 'X chromosome' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 2558 riferimenti
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    1. Arlt, MF; Miller, DE; Beer, DG; Glover, TW
      Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells

      GENES CHROMOSOMES & CANCER
    2. Zuccotti, M; Boiani, M; Ponce, R; Guizzardi, S; Scandroglio, R; Garagna, S; Redi, CA
      Mouse Xist expression begins at zygotic genome activation and is timed by a zygotic clock

      MOLECULAR REPRODUCTION AND DEVELOPMENT
    3. Guthrie, HD; Johnson, LA; Garrett, WM; Welch, GR; Dobrinsky, JR
      Flow cytometric sperm sorting: Effects of varying laser power on embryo development in swine

      MOLECULAR REPRODUCTION AND DEVELOPMENT
    4. Lawson, LJ; Hewitt, GM
      Comparison of substitution rates in ZFX and ZFY introns of sheep and goat related species supports the hypothesis of male-biased mutation rates

      JOURNAL OF MOLECULAR EVOLUTION
    5. Lockshin, MD
      Genome and hormones: Gender differences in physiology - Invited review: Sex ratio and rheumatic disease

      JOURNAL OF APPLIED PHYSIOLOGY
    6. Ostrer, H
      Genome and hormones: Gender differences in physiology - Invited review: Sex-based differences in gene expression

      JOURNAL OF APPLIED PHYSIOLOGY
    7. Lockshin, MD
      Sex ratio and rheumatic disease

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    8. Brown, CJ
      Equality of the sexes: Mammalian dosage compensation

      SEMINARS IN REPRODUCTIVE MEDICINE
    9. McElreavey, K; Cortes, LS
      X-Y translocations and sex differentiation

      SEMINARS IN REPRODUCTIVE MEDICINE
    10. Leppig, KA; Disteche, CM
      Ring X and other structural X chromosome abnormalities: X inactivation andphenotype

      SEMINARS IN REPRODUCTIVE MEDICINE
    11. Robinson, WP; Beever, C; Brown, CJ; Stephenson, MD
      Skewed X inactivation and recurrent spontaneous abortion

      SEMINARS IN REPRODUCTIVE MEDICINE
    12. Cremer, T; Cremer, C
      Chromosome territories, nuclear architecture and gene regulation in mammalian cells

      NATURE REVIEWS GENETICS
    13. Zarkower, D
      Establishing sexual dimorphism: Conservation amidst diversity?

      NATURE REVIEWS GENETICS
    14. Lahn, BT; Pearson, NM; Jegalian, K
      The human Y chromosome, in the light of evolution

      NATURE REVIEWS GENETICS
    15. Emanuel, BS; Shaikh, TH
      Segmental duplications: An 'expanding' role in genomic instability and disease

      NATURE REVIEWS GENETICS
    16. Montgomery, GW; Galloway, SM; Davis, GH; McNatty, KP
      Genes controlling ovulation rate in sheep

      REPRODUCTION
    17. Akhtar, A; Becker, PB
      The histone H4 acetyltransferase MOF uses a C2HC zinc finger for substraterecognition

      EMBO REPORTS
    18. Hsu, T; McRackan, D; Vincent, TS; de Couet, HG
      Drosophila Pin1 prolyl isomerase Dodo is a MAP kinase signal responder during oogenesis

      NATURE CELL BIOLOGY
    19. Tumbar, T; Belmont, AS
      Interphase movements of a DNA chromosome region modulated by VP16 transcriptional activator

      NATURE CELL BIOLOGY
    20. Edwards, J; Krishna, NS; Mukherjee, R; Watters, AD; Underwood, MA; Bartlett, JMS
      Amplification of the androgen receptor may not explain the development of androgen-independent prostate cancer

      BJU INTERNATIONAL
    21. Massat, I; Souery, D; Del-Favero, J; Oruc, L; Jakovljevic, M; Folnegovic, V; Adolfsson, R; Kaneva, R; Papadimitriou, G; Dikeos, D; Jazin, E; Milanova, V; Van Broeckhoven, C; Mendlewicz, J
      Lack of association between GABRA3 and unipolar affective disorder: a multicentre study

      INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY
    22. Shinka, T; Naroda, T; Tamura, T; Sasahara, K; Nakahori, Y
      A rapid and simple method for sex identification by heteroduplex analysis,using denaturing high-performance liquid chromatography (DHPLC)

      JOURNAL OF HUMAN GENETICS
    23. Uehara, S; Sato, K; Hashiyada, M; Obara, Y; Matsuzaki, S; Nata, M; Okamura, K
      X chromosome inactivation patterns in 45,X/46,XX mosaics

      JOURNAL OF HUMAN GENETICS
    24. Erdmann, VA; Barciszewska, MZ; Hochberg, A; de Groot, N; Barciszewski, J
      Regulatory RNAs

      CELLULAR AND MOLECULAR LIFE SCIENCES
    25. Sutherland, JE; Peng, W; Zhang, QW; Costa, M
      The histone deacetylase inhibitor trichostatin A reduces nickel-induced gene silencing in yeast and mammalian cells

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    26. Bukvic, N; Gentile, M; Susca, F; Fanelli, M; Serio, G; Buonadonna, L; Capurso, A; Guanti, G
      Sex chromosome loss, micronuclei, sister chromatid exchange and aging: a study including 16 centenarians

      MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
    27. Leach, NT; Jackson-Cook, C
      The application of spectral karyotyping (SKY) and fluorescent in situ hybridization (FISH) technology to determine the chromosomal content(s) of micronuclei

      MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
    28. Abir, R; Fisch, B; Nahum, R; Orvieto, R; Nitke, S; Ben Rafael, Z
      Turner's syndrome and fertility: current status and possible putative prospects

      HUMAN REPRODUCTION UPDATE
    29. Satta, Y
      Comparison of DNA and protein polymorphisms between humans and chimpanzees

      GENES & GENETIC SYSTEMS
    30. Vasques, LR; Pereira, LV
      Allele-specific X-linked gene activity in normal human cells assayed by expressed single nucleotide polymorphisms (cSNPs)

      DNA RESEARCH
    31. Pesch, K; Tomiuk, J; Broghammer, M; Zrenner, E; Apfelstedt-Sylla, E; Jacobi, FK; Wissinger, B; Pusch, CM
      Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disorders

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    32. Suka, N; Suka, Y; Carmen, AA; Wu, JS; Grunstein, M
      Highly specific antibodies determine histone acetylation site usage in yeast heterochromatin and euchromatin

      MOLECULAR CELL
    33. Florence, B; Faller, DV
      You BET-CHA: A novel family of transcriptional regulators

      FRONTIERS IN BIOSCIENCE
    34. Caceres, M; Puig, M; Ruiz, A
      Molecular characterization of two natural hotspots in the Drosophila buzzatii genome induced by transposon insertions

      GENOME RESEARCH
    35. Maddox, JF; Davies, KP; Crawford, AM; Hulme, DJ; Vaiman, D; Cribiu, EP; Freking, BA; Beh, KJ; Cockett, NE; Kang, N; Riffkin, CD; Drinkwater, R; Moore, SS; Dodds, KG; Lumsden, JM; van Stijn, TC; Phua, SH; Adelson, DL; Burkin, HR; Broom, JE; Buitkamp, J; Cambridge, L; Cushwa, WT; Gerard, E; Galloway, SM; Harrison, B; Hawken, RJ; Hiendleder, S; Henry, HM; Medrano, JF; Paterson, KA; Schibler, L; Stone, RT; van Hest, B
      An enhanced linkage map of the sheep genome comprising more than 1000 loci

      GENOME RESEARCH
    36. Nesterova, TB; Slobodyanyuk, SY; Elisaphenko, EA; Shevchenko, AI; Johnston, C; Pavlova, ME; Rogozin, IB; Kolesnikov, NN; Brockdorff, N; Zakian, SM
      Characterization of the genomic Xist locus in rodents reveals conservationof overall gene structure and tandem repeats but rapid evolution of uniquesequence

      GENOME RESEARCH
    37. Paulsen, M; Takada, S; Youngson, NA; Benchaib, M; Charlier, C; Segers, K; Georges, M; Ferguson-Smith, AC
      Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2-H19 region

      GENOME RESEARCH
    38. Gianfrancesco, F; Sanges, R; Esposito, T; Tempesta, S; Rao, E; Rappold, G; Archidiacono, N; Graves, JAM; Forabosco, A; D'Urso, M
      Differential divergence of three human pseudoautosomal genes and their mouse homologs: Implications for sex chromosome evolution

      GENOME RESEARCH
    39. Urnov, FD; Wolffe, AP
      Above and within the genome: Epigenetics past and present

      JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA
    40. Mielnicki, LM; Asch, HL; Asch, BB
      Genes, chromatin, and breast cancer: An epigenetic tale

      JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA
    41. Fischer, A
      Primary T-lymphocyte immunodeficiencies

      CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY
    42. Debinski, W; Slagle-Webb, B; Achen, MG; Stacker, SA; Tulchinsky, E; Gillespie, GY; Gibo, DM
      VEGF-D is an x-linked/AP-1 regulated putative onco-angiogen in human glioblastoma multiforme

      MOLECULAR MEDICINE
    43. Zinn, AR
      The X chromosome and the ovary

      JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION
    44. Jungbluth, AA; King, R; Fisher, DE; Iversen, K; Coplan, K; Kolb, D; Williamson, B; Chen, YT; Stockert, E; Old, LJ; Busam, KJ
      Immunohistochemical and reverse transcription-polymerase chain reaction expression analysis of tyrosinase and microphthalmia-associated transcriptionfactor in angiomyolipomas

      APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY
    45. Kawaguchi, TK; Skaletsky, H; Brown, LG; Minx, PJ; Cordum, HS; Waterston, RH; Wilson, RK; Silber, S; Oates, R; Rozen, S; Page, DC
      The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men

      NATURE GENETICS
    46. Brunkow, ME; Jeffery, EW; Hjerrild, KA; Paeper, B; Clark, LB; Yasayko, SA; Wilkinson, JE; Galas, D; Ziegler, SF; Ramsdell, F
      Disruption of a new forkhead/winged-helix protein, scurfin, results in thefatal lymphoproliferative disorder of the scurfy mouse

      NATURE GENETICS
    47. Diaz-Cano, SJ; Blanes, A; Wolfe, HJ
      PCR techniques for clonality assays

      DIAGNOSTIC MOLECULAR PATHOLOGY
    48. McBurney, MW; Lau, S; Jardine, K; Yang, XF; Davies, B
      Reexpression of a cluster of silenced transgenes is associated with their rearrangement

      GENES CHROMOSOMES & CANCER
    49. Taneja, KL; Chavez, EA; Coull, J; Lansdorp, PM
      Multicolor fluorescence in situ hybridization with peptide nucleic acid probes for enumeration of specific chromosomes in human cells

      GENES CHROMOSOMES & CANCER
    50. Levy, A
      Monoclonality of endocrine tumours: what does it mean?

      TRENDS IN ENDOCRINOLOGY AND METABOLISM
    51. Konyukhov, BV; Platonov, ES
      Genomic imprinting in mammals

      RUSSIAN JOURNAL OF GENETICS
    52. Vourc'h, P; Bienvenu, T; Beldjord, C; Chelly, J; Barthelemy, C; Muh, JP; Andres, C
      No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients

      EUROPEAN JOURNAL OF HUMAN GENETICS
    53. Girard, M; Couvert, P; Carrie, A; Tardieu, M; Chelly, J; Beldjord, C; Bienvenu, T
      Parental origin of de novo MECP2 mutations in Rett syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    54. Chiurazzi, P; Hamel, BCJ; Neri, G
      XLMR genes: update 2000

      EUROPEAN JOURNAL OF HUMAN GENETICS
    55. Kim, HS; Takenaka, O
      Phylogeny of SINE-R retroposons in Asian apes

      MOLECULES AND CELLS
    56. Piumi, F; Vaiman, D; Cribiu, EP; Guerin, B; Humblot, P
      Specific cytogenetic labeling of bovine spermatozoa bearing X or Y chromosomes using fluorescent in situ hybridization (FISH)

      GENETICS SELECTION EVOLUTION
    57. Kuroda, Y; Arai, N; Arita, M; Teranishi, M; Hori, T; Harata, M; Mizuno, S
      Absence of Z-chromosome inactivation for five genes in male chickens

      CHROMOSOME RESEARCH
    58. Ball, AR; Yokomori, K
      The structural maintenance of chromosomes (SMC) family of proteins in mammals

      CHROMOSOME RESEARCH
    59. Kuroiwa, A; Tsuchiya, K; Watanabe, T; Hishigaki, H; Takahashi, E; Namikawa, T; Matsuda, Y
      Conservation of the rat X chromosome gene order in rodent species

      CHROMOSOME RESEARCH
    60. Meguro, M; Mitsuya, K; Nomura, N; Kohda, M; Kashiwagi, A; Nishigaki, R; Yoshioka, H; Nakao, M; Oishi, M; Oshimura, M
      Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes

      HUMAN MOLECULAR GENETICS
    61. LaSalle, JM; Goldstine, J; Balmer, D; Greco, CM
      Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry

      HUMAN MOLECULAR GENETICS
    62. Wan, MM; Zhao, KJ; Lee, SSJ; Francke, U
      MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome

      HUMAN MOLECULAR GENETICS
    63. Ellaway, C; Christodoulou, J
      Rett syndrome: clinical characteristics and recent genetic advances

      DISABILITY AND REHABILITATION
    64. Jenuwein, T
      Re-SET-ting heterochromatin by histone methyltransferases

      TRENDS IN CELL BIOLOGY
    65. Ellaway, CJ; Badawi, N; Raffaele, L; Christodoulou, J; Leonard, H
      A case of multiple congenital anomalies in association with Rett syndrome confirmed by MECP2 mutation screening

      CLINICAL DYSMORPHOLOGY
    66. Lammer, EJ; Punglia, DR; Fuchs, AE; Rowe, AG; Cotter, PD
      Inherited duplication of Xq27.2 -> qter: phenocopy of infantile Prader-Willi syndrome

      CLINICAL DYSMORPHOLOGY
    67. McQueen, HA; McBride, D; Miele, G; Bird, AP; Clinton, M
      Dosage compensation in birds

      CURRENT BIOLOGY
    68. Aravin, AA; Naumova, NM; Tulin, AV; Vagin, VV; Rozovsky, YM; Gvozdev, VA
      Double-stranded RNA-mediated silencing of genomic tandem repeats and transposable elements in the D-melanogaster germline

      CURRENT BIOLOGY
    69. Harris, EE; Hey, J
      Human populations show reduced DNA sequence variation at the Factor IX locus

      CURRENT BIOLOGY
    70. Romero, NB; De Lonlay, P; Llense, S; Leturcq, F; Touati, G; Urtizberea, JA; Saudubray, JM; Munnich, A; Kaplan, JC; Recan, D
      Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomaticcarrier with 'de novo' duplication of dystrophin gene

      NEUROMUSCULAR DISORDERS
    71. Aquadro, CF; DuMont, VB; Reed, FA
      Genome-wide variation in the human and fruitfly: a comparison

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    72. Kiemer, AK; Takeuchi, K; Quinlan, MP
      Identification of genes involved in epithelial-mesenchymal transition and tumor progression

      ONCOGENE
    73. Ladanyi, M
      Fusions of the SYT and SSX genes in synovial sarcoma

      ONCOGENE
    74. Pflumm, MF; Botchan, MR
      Orc mutants arrest in metaphase with abnormally condensed chromosomes

      DEVELOPMENT
    75. Strunkelnberg, M; Bonengel, B; Moda, LM; Hertenstein, A; de Couet, HG; Ramos, RGP; Fischbach, KF
      rst and its paralogue kirre act redundantly during embryonic muscle development in Drosophila

      DEVELOPMENT
    76. Vacca, M; Filippini, F; Budillon, A; Rossi, V; Mercadante, G; Manzati, E; Gualandi, F; Bigoni, S; Trabanelli, C; Pini, G; Calzolari, E; Ferlini, A; Meloni, I; Hayek, G; Zappella, M; Renieri, A; D'Urso, M; D'Esposito, M; MacDonald, F; Kerr, A; Dhanjal, S; Hulten, M
      Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females

      JOURNAL OF MOLECULAR MEDICINE-JMM
    77. Vidal, S; Kovacs, K; Horvath, E; Scheithauer, BW; Kuroki, T; Lloyd, RV
      Microvessel density in pituitary adenomas and carcinomas

      VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY
    78. Chen, TC; Chou, TB; Ng, KF; Hsieh, LL; Chou, YHW
      Hepatocellular carcinoma associated with focal nodular hyperplasia - Report of a case with clonal analysis

      VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY
    79. Cheverud, JM; Vaughn, TT; Pletscher, LS; Peripato, AC; Adams, ES; Erikson, CF; King-Ellison, KJ
      Genetic architecture of adiposity in the cross of LG/J and SM/J inbred mice

      MAMMALIAN GENOME
    80. Edelmann, J; Szibor, R
      DXS101: a highly polymorphic X-linked STR

      INTERNATIONAL JOURNAL OF LEGAL MEDICINE
    81. Malou, E; Gekas, J; Troucelier-Lucas, V; Mornet, E; Razafimanantsoa, L; Cuvelier, B; Mathieu, M; Thepot, F
      X-linked recessive chondrodysplasia punctata: cytogenetic and molecular biology study.

      ARCHIVES DE PEDIATRIE
    82. Karasawa, M; Tsukamoto, N; Yamane, A; Okamoto, K; Maehara, T; Yokohama, A; Nojima, Y; Omine, M
      Analysis of the distribution of CAG repeats and X-chromosome inactivation status of HUMARA gene in healthy female subjects using improved fluorescence-based assay

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    83. Boultwood, J; Wainscoat, JS
      Clonality in the myelodysplastic syndromes

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    84. Tefferi, A
      The pathogenesis of chronic myeloproliferative diseases

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    85. Johansson, C; Jansson, M; Linner, L; Yuan, QP; Pedersen, NL; Blackwood, D; Barden, N; Kelsoe, J; Schalling, M
      Genetics of affective disorders

      EUROPEAN NEUROPSYCHOPHARMACOLOGY
    86. Clement, Y; Lepicard, E; Chapouthier, G
      An animal model for the study of the genetic bases of behaviour in men: the multiple marker strains (MMS)

      EUROPEAN PSYCHIATRY
    87. Izumi, Y; Tatsumi, K; Okamoto, S; Ogawa, T; Hosokawa, A; Matsuo, T; Kato, Y; Fukui, H; Amino, N
      Analysis of the KAL1 gene in 19 Japanese patients with Kallmann syndrome

      ENDOCRINE JOURNAL
    88. Guo, ZM; Wu, F; Asplund, A; Hu, XR; Mazurenko, N; Kisseljov, F; Ponten, J; Wilander, E
      Analysis of intratumoral heterogeneity of chromosome 3p deletions and genetic evidence of polyclonal origin of cervical squamous carcinoma

      MODERN PATHOLOGY
    89. Mumm, S; Herrera, L; Waeltz, PW; Scardovi, A; Nagaraja, R; Esposito, T; Schlessinger, D; Rocchi, M; Forabosco, A
      X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes

      GENOMICS
    90. Mahesh, G; Ramachandra, NB; Ranganath, HA
      Autoradiographic study of transcription and dosage compensation in the sexand neo-sex chromosome of Drosophila nasuta nasuta and Drosophila nasuta albomicans

      GENOME
    91. Ausio, J; Abbott, DW; Wang, XY; Moore, SC
      Histone variants and histone modifications: A structural perspective

      BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE
    92. Schachter, F; Foulon, M; Poulain, M
      Color vision anomalies and the genetics of aging.

      COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE III-SCIENCES DE LA VIE-LIFE SCIENCES
    93. Quintana-Murci, T; Jamain, S; Fellous, M
      The origin and evolution of mammalian sex chromosomes.

      COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE III-SCIENCES DE LA VIE-LIFE SCIENCES
    94. Sanjuan, R; Marin, I
      Tracing the origin of the compensasome: Evolutionary history of DEAH helicase and MYST acetyltransferase gene families

      MOLECULAR BIOLOGY AND EVOLUTION
    95. Takahata, N; Lee, SH; Satta, Y
      Testing multiregionality of modern human origins

      MOLECULAR BIOLOGY AND EVOLUTION
    96. Yu, N; Fu, YX; Sambuughin, N; Ramsay, M; Jenkins, T; Leskinen, E; Patthy, L; Jorde, LB; Kuromori, T; Li, WH
      Global patterns of human DNA sequence variation in a 10-kb region on chromosome 1

      MOLECULAR BIOLOGY AND EVOLUTION
    97. Lercher, MJ; Williams, EJB; Hurst, LD
      Local similarity in evolutionary rates extends over whole chromosomes in human-rodent and mouse-rat comparisons: Implications for understanding the mechanistic basis of the male mutation bias

      MOLECULAR BIOLOGY AND EVOLUTION
    98. Makinen, A; Suojala, L; Niini, T; Katila, T; Tozaki, T; Miyake, YI; Hasegawa, T
      X chromosome detection in an XO mare using a human X paint probe, and PCR detection of SRY and amelogenin genes in 3 XY mares

      EQUINE VETERINARY JOURNAL
    99. Bernasconi, S; Mariani, S; Falcinelli, C; Milioli, S; Iughetti, L; Forabosco, A
      SHOX gene in Leri-Weill syndrome and in idiopathic short stature

      JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
    100. Pascual-Castroviejo, I; Pascual-Pascual, SI; Viano, J; Martinez, V; Palencia, R
      Unilateral polymicrogyria: a common cause of hemiplegia of prenatal origin

      BRAIN & DEVELOPMENT


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Documento generato il 23/10/20 alle ore 08:02:52