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1 Ergebnisse
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Clinical phenotype of the recurrent 1q21.1 copy-number vari..:
Bernier, Raphael
;
Steinman, Kyle J
;
Reilly, Beau
...
qt6j06n700. , 2016
Link:
https://escholarship.org/uc/item/6j06n700
RT Journal T1
Clinical phenotype of the recurrent 1q21.1 copy-number variant
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt6j06n700&Exemplar=1&LAN=DE A1 Bernier, Raphael A1 Steinman, Kyle J A1 Reilly, Beau A1 Wallace, Arianne Stevens A1 Sherr, Elliott H A1 Pojman, Nicholas A1 Mefford, Heather C A1 Gerdts, Jennifer A1 Earl, Rachel A1 Hanson, Ellen A1 Goin-Kochel, Robin P A1 Berry, Leandra A1 Kanne, Stephen A1 Snyder, LeeAnne Green A1 Spence, Sarah A1 Ramocki, Melissa B A1 Evans, David W A1 Spiro, John E A1 Martin, Christa L A1 Ledbetter, David H A1 Chung, Wendy K A1 Simons VIP consortium PB eScholarship, University of California YR 2016 K1 Simons VIP consortium K1 Chromosomes K1 Human K1 Pair 1 K1 Humans K1 Chromosome Disorders K1 Chromosome Deletion K1 Registries K1 Neuropsychological Tests K1 Phenotype K1 Adult K1 Middle Aged K1 Child K1 Preschool K1 Female K1 Male K1 Young Adult K1 DNA Copy Number Variations K1 Chromosome Duplication K1 Autism K1 Intellectual and Developmental Disabilities (IDD) K1 Mental Health K1 Pediatric K1 Genetics K1 Neurosciences K1 Genetic Testing K1 Clinical Research K1 Brain Disorders K1 Behavioral and Social Science K1 autism spectrum disorder K1 copy-number variation K1 developmental disability K1 1q21.1 deletion K1 1q21.1 duplication K1 Clinical Sciences K1 Genetics & Heredity JF qt6j06n700 LK http://dx.doi.org/https://escholarship.org/uc/item/6j06n700 DO https://escholarship.org/uc/item/6j06n700 SF ELIB - SuUB Bremen
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