التفاصيل البيبلوغرافية
| العنوان: |
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes |
| المؤلفون: |
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., Laulund, L. W., Pellecchia, G., Lamoureux, S., Deshpande, C., Clayton-Smith, J., White, A. C., Leather, S., Trounce, J., Melanie Bedford, H., 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., Brian Lowry, R., Zwaigenbaum, L., Mandyam, D., Wei, J., MacDonald, J. R., Howe, J. L., Nalpathamkalam, T., Wang, Z., Tolson, D. |
| المصدر: |
Human Molecular Genetics ; volume 23, issue 10, page 2752-2768 ; ISSN 0964-6906 1460-2083 |
| بيانات النشر: |
Oxford University Press (OUP) |
| سنة النشر: |
2013 |
| نوع الوثيقة: |
article in journal/newspaper |
| اللغة: |
English |
| DOI: |
10.1093/hmg/ddt669 |
| الإتاحة: |
https://doi.org/10.1093/hmg/ddt669Test
http://academic.oup.com/hmg/article-pdf/23/10/2752/1698409/ddt669.pdfTest |
| رقم الانضمام: |
edsbas.87BA708C |
| قاعدة البيانات: |
BASE |
