دورية أكاديمية

Assessment of 2q23.1 Microdeletion Syndrome Implicates MBD5 as a Single Causal Locus of Intellectual Disability, Epilepsy, and Autism Spectrum Disorder

التفاصيل البيبلوغرافية
العنوان: Assessment of 2q23.1 Microdeletion Syndrome Implicates MBD5 as a Single Causal Locus of Intellectual Disability, Epilepsy, and Autism Spectrum Disorder
المؤلفون: Talkowski, Michael E., Mullegama, Sureni V., Rosenfeld, Jill A., van Bon, Bregje W.M., Shen, Yiping, Repnikova, Elena A., Gastier-Foster, Julie, Thrush, Devon Lamb, Kathiresan, Sekar, Ruderfer, Douglas M., Chiang, Colby, Hanscom, Carrie, Ernst, Carl, Lindgren, Amelia M., Morton, Cynthia C., An, Yu, Astbury, Caroline, Brueton, Louise A., Lichtenbelt, Klaske D., Ades, Lesley C., Fichera, Marco, Romano, Corrado, Innis, Jeffrey W., Williams, Charles A., Bartholomew, Dennis, Van Allen, Margot I., Parikh, Aditi, Zhang, Lilei, Wu, Bai-Lin, Pyatt, Robert E., Schwartz, Stuart, Shaffer, Lisa G., de Vries, Bert B.A., Gusella, James F., Elsea, Sarah H.
المصدر: The American Journal of Human Genetics ; volume 89, issue 4, page 551-563 ; ISSN 0002-9297
بيانات النشر: Elsevier BV
سنة النشر: 2011
المجموعة: ScienceDirect (Elsevier - Open Access Articles via Crossref)
مصطلحات موضوعية: Genetics (clinical), Genetics
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1016/j.ajhg.2011.09.011
الإتاحة: https://doi.org/10.1016/j.ajhg.2011.09.011Test
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https://api.elsevier.com/content/article/PII:S0002929711004010?httpAccept=text/plainTest
حقوق: https://www.elsevier.com/tdm/userlicense/1.0Test/ ; https://www.elsevier.com/open-access/userlicense/1.0Test/
رقم الانضمام: edsbas.3C0FF677
قاعدة البيانات: BASE