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1 Ergebnisse
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A rare genomic duplication in 2p14 underlies autosomal domi..:
Oiticica, Jeanne
;
Mingroni-Netto, Regina C
;
Bento, Ricardo F
...
Human Molecular Genetics. 29 (2020) 9 - p. 1520-1536 , 2020
Link:
https://doi.org/10.1093/hmg/ddaa075
RT Journal T1
A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_hmg_ddaa075&Exemplar=1&LAN=DE A1 Oiticica, Jeanne A1 Mingroni-Netto, Regina C A1 Bento, Ricardo F A1 Grillet, Nicolas A1 Jagger, Daniel J A1 Grasel, Signe S A1 Beck, Roberto M O A1 Vasconcelos, Laura G A1 Borges, Vinícius M A1 Sonoda, Cindy Y A1 Nascimento, Larissa R A1 Pedroso-Campos, Vinicius A1 Sampaio-Silva, Juliana A1 Zebarjadi, Navid A1 Ouyang, Ellen A1 Trouillet, Alix A1 Kitajima, Joao P A1 Levy, Débora A1 Batissoco, Ana C A1 Vieira-Silva, Gleiciele A A1 Lezirovitz, Karina PB Oxford University Press (OUP) YR 2020 SN 0964-6906 SN 1460-2083 JF Human Molecular Genetics VO 29 IS 9 SP 1520 OP 1536 LK http://dx.doi.org/https://doi.org/10.1093/hmg/ddaa075 DO https://doi.org/10.1093/hmg/ddaa075 SF ELIB - SuUB Bremen
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