يعرض 1 - 10 نتائج من 13 نتيجة بحث عن '"Nardone A."', وقت الاستعلام: 0.86s تنقيح النتائج
  1. 1

    المصدر: PLoS Pathogens
    PLoS Pathogens, Vol 16, Iss 9, p e1008855 (2020)

  2. 2
  3. 3
  4. 4
  5. 5

    المصدر: Lionel, A C, Tammimies, K, Vaags, A K, Rosenfeld, J A, Ahn, J W, Merico, D, Noor, A, Runke, C K, Pillalamarri, V K, Carter, M T, Gazzellone, M J, Thiruvahindrapuram, B, Fagerberg, C R, Laulund, L W, Pellecchia, G, Lamoureux, S, Deshpande, C, Clayton-Smith, J, White, A C, Leather, S, Trounce, J, Bedford, H M, Hatchwell, E, Eis, P S, Yuen, R K C, Walker, S, Uddin, M, Geraghty, M T, Nikkel, S M, Tomiak, E M, Fernandez, B A, Soreni, N, Crosbie, J, Arnold, P D, Schachar, R J, Roberts, W, Paterson, A D, So, J, Szatmari, P, Chrysler, C, Woodbury-Smith, M, Lowry, R B, Zwaigenbaum, L, Mandyam, D, Wei, J, Macdonald, J R, Howe, J L, Nalpathamkalam, T, Wang, Z, Tolson, D, Cobb, D S, Wilks, T M, Sorensen, M J, Bader, P I, An, Y, Wu, B-L, Musumeci, S A, Romano, C, Postorivo, D, Nardone, A M, Della Monica, M, Scarano, G, Zoccante, L, Novara, F, Zuffardi, O, Ciccone, R, Antona, V, Carella, M, Zelante, L, Cavalli, P, Poggiani, C, Cavallari, U, Argiropoulos, B, Chernos, J, Brasch-Andersen, C, Speevak, M, Fichera, M, Ogilvie, C M, Shen, Y, Hodge, J C, Talkowski, M E, Stavropoulos, D J, Marshall, C R & Scherer, S W 2014, ' Disruption of the ASTN2 / TRIM32 locus at 9q33.1 is a risk factor in males for Autism Spectrum Disorders, ADHD and other neurodevelopmental phenotypes ', Human Molecular Genetics, vol. 23, no. 10, ddt669, pp. 2752-2768 . https://doi.org/10.1093/hmg/ddt669Test
    Human molecular genetics, vol 23, iss 10

    مصطلحات موضوعية: Male, Receptors, Cell Surface/genetics, Autism, Child Development Disorders, Pervasive/genetics, Gene Expression, Genome-wide association study, Medical and Health Sciences, Tripartite Motif Proteins, Risk Factors, Receptors, 2.1 Biological and endogenous factors, Protein Isoforms, Nerve Tissue Proteins/genetics, Copy-number variation, Aetiology, Child, Genetics (clinical), Sequence Deletion, Pediatric, Genetics & Heredity, Genetics, education.field_of_study, Single Nucleotide, Articles, General Medicine, Exons, Biological Sciences, Mental Health, Phenotype, Autism spectrum disorder, Organ Specificity, Cerebellar cortex, Child, Preschool, Cell Surface, Speech delay, Female, medicine.symptom, Transcription Initiation Site, Attention Deficit Disorder with Hyperactivity/genetics, Chromosomes, Human, Pair 9, Human, Pair 9, Adult, Pediatric Research Initiative, Child Development Disorders, Adolescent, DNA Copy Number Variations, Intellectual and Developmental Disabilities (IDD), Ubiquitin-Protein Ligases, Population, Transcription Factors/genetics, Nerve Tissue Proteins, Receptors, Cell Surface, Biology, Polymorphism, Single Nucleotide, Chromosomes, Young Adult, Clinical Research, Protein Isoforms/genetics, Behavioral and Social Science, medicine, Attention deficit hyperactivity disorder, Humans, Genetic Predisposition to Disease, Polymorphism, Preschool, education, Molecular Biology, Genetic Association Studies, Pervasive, Glycoproteins, Human Genome, Neurosciences, Infant, Newborn, Glycoproteins/genetics, Infant, Newborn, medicine.disease, Brain Disorders, Attention Deficit Disorder with Hyperactivity, Child Development Disorders, Pervasive, Case-Control Studies, Transcription Factors

    وصف الملف: application/pdf

  6. 6
  7. 7
  8. 8
    دورية أكاديمية
  9. 9
  10. 10
    دورية أكاديمية