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1 Ergebnisse
1
De Novo Insertions and Deletions of Predominantly Paternal ..:
Dong, Shan
;
Walker, Michael F
;
Carriero, Nicholas J
...
qt1qh3s2x6. , 2014
Link:
https://escholarship.org/uc/item/1qh3s2x6
RT Journal T1
De Novo Insertions and Deletions of Predominantly Paternal Origin Are Associated with Autism Spectrum Disorder
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt1qh3s2x6&Exemplar=1&LAN=DE A1 Dong, Shan A1 Walker, Michael F A1 Carriero, Nicholas J A1 DiCola, Michael A1 Willsey, A Jeremy A1 Ye, Adam Y A1 Waqar, Zainulabedin A1 Gonzalez, Luis E A1 Overton, John D A1 Frahm, Stephanie A1 Keaney, John F A1 Teran, Nicole A A1 Dea, Jeanselle A1 Mandell, Jeffrey D A1 Bal, Vanessa Hus A1 Sullivan, Catherine A A1 DiLullo, Nicholas M A1 Khalil, Rehab O A1 Gockley, Jake A1 Yuksel, Zafer A1 Sertel, Sinem M A1 Ercan-Sencicek, A Gulhan A1 Gupta, Abha R A1 Mane, Shrikant M A1 Sheldon, Michael A1 Brooks, Andrew I A1 Roeder, Kathryn A1 Devlin, Bernie A1 State, Matthew W A1 Wei, Liping A1 Sanders, Stephan J PB eScholarship, University of California YR 2014 K1 Biological Sciences K1 Bioinformatics and Computational Biology K1 Genetics K1 Autism K1 Human Genome K1 Intellectual and Developmental Disabilities (IDD) K1 Brain Disorders K1 Mental Health K1 Pediatric K1 Aetiology K1 2.1 Biological and endogenous factors K1 Child K1 Child Development Disorders K1 Pervasive K1 DNA K1 DNA-Binding Proteins K1 Female K1 Fragile X Mental Retardation Protein K1 Frameshift Mutation K1 GTP-Binding Proteins K1 Humans K1 Male K1 Nerve Tissue Proteins K1 Pedigree K1 Phenotype K1 Sequence Deletion K1 Sex Factors K1 Biochemistry and Cell Biology K1 Medical Physiology JF qt1qh3s2x6 LK http://dx.doi.org/https://escholarship.org/uc/item/1qh3s2x6 DO https://escholarship.org/uc/item/1qh3s2x6 SF ELIB - SuUB Bremen
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