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Genome sequencing is a sensitive first-line test to diagnos..:
Lindstrand, Anna
;
Ek, Marlene
;
Kvarnung, Malin
...
Genetics in Medicine, 1098-3600, 2022, 24:11, s. 2296-2307. , 2022
Link:
http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-19139
RT Journal T1
Genome sequencing is a sensitive first-line test to diagnose individuals with intellectual disability
UL https://suche.suub.uni-bremen.de/peid=base-ftlinkoepinguniv:oai:DiVA.org:liu-191398&Exemplar=1&LAN=DE A1 Lindstrand, Anna A1 Ek, Marlene A1 Kvarnung, Malin A1 Anderlid, Britt-Marie A1 Bjoerck, Erik A1 Carlsten, Jonas A1 Eisfeldt, Jesper A1 Grigelioniene, Giedre A1 Gustavsson, Peter A1 Hammarsjoe, Anna A1 Helgadottir, Hafdis T A1 Hellstroem-Pigg, Maritta A1 Kuchinskaya, Ekaterina A1 Lagerstedt-Robinson, Kristina A1 Levin, Lars-Åke A1 Lieden, Agne A1 Lindeloef, Hillevi A1 Malmgren, Helena A1 Nilsson, Daniel A1 Svensson, Eva A1 Paucar, Martin A1 Sahlin, Ellika A1 Tesi, Bianca A1 Tham, Emma A1 Winberg, Johanna A1 Winerdal, Max A1 Wincent, Josephine A1 Soller, Maria Johansson A1 Pettersson, Maria A1 Nordgren, Ann PB Linköpings universitet, Avdelningen för samhälle och hälsa; Linköpings universitet, Medicinska fakulteten; Karolinska Inst, Sweden; Karolinska Univ Hosp, Sweden; Karolinska Inst, Sweden; Karolinska Univ Hosp, Sweden; Karolinska Inst, Sweden; Karolinska Univ Hosp, Sweden; ELSEVIER SCIENCE INC YR 2022 K1 Chromosomal microarray K1 Clinical diagnostics K1 FMR1 analysis K1 Genome sequencing K1 Intellectual disability K1 Medical Genetics K1 Medicinsk genetik JF Genetics in Medicine, 1098-3600, 2022, 24:11, s. 2296-2307 LK http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-191398 DO http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-191398 SF ELIB - SuUB Bremen
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