التفاصيل البيبلوغرافية
| العنوان: |
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression |
| المؤلفون: |
Lowther, Chelsea, Speevak, Marsha, Armour, Christine M., Goh, Elaine S., Graham, Gail E., Li, Chumei, Zeesman, Susan, Nowaczyk, Malgorzata J.M., Schultz, Lee-Anne, Morra, Antonella, Nicolson, Rob, Bikangaga, Peter, Samdup, Dawa, Zaazou, Mostafa, Boyd, Kerry, Jung, Jack H., Siu, Victoria, Rajguru, Manjulata, Goobie, Sharan, Tarnopolsky, Mark A., Prasad, Chitra, Dick, Paul T., Hussain, Asmaa S., Walinga, Margreet, Reijenga, Renske G., Gazzellone, Matthew, Lionel, Anath C., Marshall, Christian R., Scherer, Stephen W., Stavropoulos, Dimitri J., McCready, Elizabeth, Bassett, Anne S. |
| المصدر: |
Genetics in Medicine ; volume 19, issue 1, page 53-61 ; ISSN 1098-3600 |
| بيانات النشر: |
Elsevier BV |
| سنة النشر: |
2017 |
| المجموعة: |
ScienceDirect (Elsevier - Open Access Articles via Crossref) |
| مصطلحات موضوعية: |
Genetics (clinical) |
| نوع الوثيقة: |
article in journal/newspaper |
| اللغة: |
English |
| DOI: |
10.1038/gim.2016.54 |
| الإتاحة: |
https://doi.org/10.1038/gim.2016.54Test
http://www.nature.com/articles/gim201654.pdfTest
http://www.nature.com/articles/gim201654Test
https://api.elsevier.com/content/article/PII:S1098360021015318?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S1098360021015318?httpAccept=text/plainTest |
| حقوق: |
https://www.elsevier.com/tdm/userlicense/1.0Test/ ; http://www.elsevier.com/open-access/userlicense/1.0Test/ ; http://www.springer.com/tdmTest |
| رقم الانضمام: |
edsbas.9961135E |
| قاعدة البيانات: |
BASE |
