A CGH array study in nonsyndromic (primary) autism patients: deletions on16p13.11, 16p11.2, 1q21.1, 2q21.1q21.2, and 8p23.1-Reference-Cited by-同舟云学术

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A CGH array study in nonsyndromic (primary) autism patients: deletions on16p13.11, 16p11.2, 1q21.1, 2q21.1q21.2, and 8p23.1

Published:2015 Issue: Volume:45 Page:313-319
ISSN:1300-0144
Container-title:TURKISH JOURNAL OF MEDICAL SCIENCES
language:
Short-container-title:Turk J Med Sci

Author:

GÜMÜŞLÜ Kudret Esen,SAVLI Hakan,SÜNNETÇİ Deniz,ÇİNE Naci,KARA Bülent,EREN KESKİN Seda,AKKOYUNLU Ramis Ufuk

Publisher

The Scientific and Technological Research Council of Turkey (TUBITAK-ULAKBIM)

Subject

General Medicine

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. 16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-up;BMC Pregnancy and Childbirth;2022-12-07

2. Rrn3 gene knockout affects ethanol-induced locomotion in adult heterozygous zebrafish;Psychopharmacology;2022-01-10

3. Increased Diagnostic Yield of Array Comparative Genomic Hybridization for Autism Spectrum Disorder in One Institution in Taiwan;Medicina;2021-12-22

4. Coexistence of Fragile-X Syndrome, 8p23.1 Deletion, and Balanced Translocation t(7;10)(p10;q24) in a Single Family;Genetic Testing and Molecular Biomarkers;2020-08-01

5. Zinc in Autism;Biometals in Neurodegenerative Diseases;2017

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