Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

BACKGROUND: Segmental duplications at breakpoints (BP4–BP5) of chromosome 15q13.2q13.3 mediate a recurrent genomic imbalance syndrome associated with mental retardation, epilepsy, and/or EEG abnormalities. PATIENTS: DNA samples from 1,445 unrelated patients submitted consecutively for clinical array...

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Κύριοι συγγραφείς: Miller, David T., Shen, Yiping, Weiss, Lauren A., Korn, Joshua, Anselm, Irina, Bridgemohan, Carolyn, Cox, Gerald F., Dickinson, Hope, Gentile, Jennifer, Harris, David J., Hegde, Vijay, Hundley, Rachel, Khwaja, Omar, Kothare, Sanjeev, Luedke, Christina, Nasir, Ramzi, Poduri, Annapurna, Prasad, Kiran, Raffalli, Peter, Reinhard, Ann, Smith, Sharon E., Sobeih, Magdi M., Soul, Janet S., Stoler, Joan, Takeoka, Masanori, Tan, Wen-Hann, Thakuria, Joseph, Wolff, Robert, Yusupov, Roman, Gusella, James F., Daly, Mark J., Wu, Bai-Lin
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: 2008
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Article
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4090085/
https://ncbi.nlm.nih.gov/pubmed/18805830
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2008.059907
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