المؤلفون: Onay H, Kacamak D, Kavasoglu AN, Akgun B, Yalcinli M, Kose S, Ozbaran B

المصدر: Balkan Journal of Medical Genetics, Vol 19, Iss 2, Pp 17-22 (2016)

مصطلحات موضوعية: autism spectrum disorder (asd), neurexin 1 (nrxn1) gene, mutation, sanger sequencing, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1311-0160

URL الوصول: https://doaj.org/article/062734b8760d4520a5682cd2caf06753

المؤلفون: Onay, H, Kacamak, D, Kavasoglu, AN, Akgun, B, Yalcinli, M, Kose, S, Ozbaran, B

المصدر: Balkan Journal of Medical Genetics; December 2016, Vol. 19 Issue: 2 p17-22, 6p

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

المؤلفون: Onay H; Department of Medical Genetics, Ege University School of Medicine, Izmir, Turkey., Kacamak D; Department of Child and Adolescent Psychiatry, Ege University School of Medicine, Izmir, Turkey., Kavasoglu AN; Department of Medical Genetics, Ege University School of Medicine, Izmir, Turkey., Akgun B; Department of Medical Genetics, Ege University School of Medicine, Izmir, Turkey., Yalcinli M; Department of Medical Genetics, Ege University School of Medicine, Izmir, Turkey., Kose S; Department of Medical Genetics, Ege University School of Medicine, Izmir, Turkey., Ozbaran B; Department of Medical Genetics, Ege University School of Medicine, Izmir, Turkey.

المصدر: Balkan journal of medical genetics : BJMG [Balkan J Med Genet] 2017 Mar 08; Vol. 19 (2), pp. 17-22. Date of Electronic Publication: 2017 Mar 08 (Print Publication: 2016).

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Sciendo Country of Publication: Poland NLM ID: 9806959 Publication Model: eCollection Cited Medium: Print ISSN: 1311-0160 (Print) Linking ISSN: 13110160 NLM ISO Abbreviation: Balkan J Med Genet Subsets: PubMed not MEDLINE