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1 Ergebnisse
1
Case Report: Whole Exome Sequencing Revealed Disease-Causin..:
Cerminara M
;
Spirito G
;
Pisciotta L
...
info:eu-repo/semantics/altIdentifier/pmid/33679889. , 2021
Link:
https://hdl.handle.net/11567/1060248
RT Journal T1
Case Report: Whole Exome Sequencing Revealed Disease-Causing Variants in Two Genes in a Patient With Autism Spectrum Disorder, Intellectual Disability, Hyperactivity, Sleep and Gastrointestinal Disturbances
UL https://suche.suub.uni-bremen.de/peid=base-ftunivgenova:oai:iris.unige.it:11567_1060248&Exemplar=1&LAN=DE A1 Cerminara M A1 Spirito G A1 Pisciotta L A1 Squillario M A1 Servetti M A1 Divizia M. T A1 Lerone M A1 Berloco B A1 Boeri S A1 Nobili L A1 Vozzi D A1 Sanges R A1 Gustincich S A1 Puliti A PB Frontiers Media S.A.; place:AVENUE DU TRIBUNAL FEDERAL 34, LAUSANNE, CH-1015, SWITZERLAND YR 2021 K1 attention deficit disorder and hyperactivity K1 autism spectrum disorder K1 gut motility disorder K1 oligenic disease K1 ORVAL K1 sleep disturbance K1 whole exome sequencing JF info:eu-repo/semantics/altIdentifier/pmid/33679889 LK http://dx.doi.org/https://hdl.handle.net/11567/1060248 DO https://hdl.handle.net/11567/1060248 SF ELIB - SuUB Bremen
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