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1 Ergebnisse
1
Exome sequencing reveals predominantly de novo variants in ..:
Järvelä, Irma
;
Määttä, Tuomo
;
Acharya, Anushree
...
10.1007/s00439-021-02268-1. , 2022
Link:
http://hdl.handle.net/10138/339008
RT Journal T1
Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland
UL https://suche.suub.uni-bremen.de/peid=base-ftunivhelsihelda:oai:helda.helsinki.fi:10138_339008&Exemplar=1&LAN=DE A1 Järvelä, Irma A1 Määttä, Tuomo A1 Acharya, Anushree A1 Leppälä, Juha A1 Jhangiani, Shalini N A1 Arvio, Maria A1 Siren, Auli A1 Kankuri-Tammilehto, Minna A1 Kokkonen, Hannaleena A1 Palomäki, Maarit A1 Varilo, Teppo A1 Fang, Mary A1 Hadley, Trevor D A1 Jolly, Angad A1 Linnankivi, Tarja A1 Paetau, Ritva A1 Saarela, Anni A1 Kälviäinen, Reetta A1 Olme, Jan A1 Nouel-Saied, Liz M A1 Cornejo-Sanchez, Diana M A1 Llaci, Lorida A1 Lupski, James R A1 Posey, Jennifer E A1 Leal, Suzanne M A1 Schrauwen, Isabelle PB Springer YR 2022 K1 Biomedicine K1 Genetics K1 developmental biology K1 physiology JF 10.1007/s00439-021-02268-1 LK http://hdl.handle.net/10138/339008 DO http://hdl.handle.net/10138/339008 SF ELIB - SuUB Bremen
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