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Case report: A de novo RASopathy-causing SHOC2 variant in a..:
Qingming Wang
;
Shuangxi Cheng
;
Youqing Fu
.
https://www.frontiersin.org/articles/10.3389/fgene.2022.1040124/full. , 2022
Link:
https://doi.org/10.3389/fgene.2022.1040124
RT Journal T1 <Title>Case report: A de novo RASopathy-causing SHOC2 variant in a Chinese girl with noonan syndrome-like with loose anagen hair</Title> UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:ef564abc0a0f4454845b8d13e89cf04c&Exemplar=1&LAN=DE A1 Qingming Wang A1 Shuangxi Cheng A1 Youqing Fu A1 Haiming Yuan PB Frontiers Media S.A. YR 2022 K1 SHOC2 K1 Noonan syndrome-like with loose anagen hair (NS/LAH) K1 short stature K1 growth hormone (GH) K1 growth hormone deficiency (GHD) K1 Genetics K1 QH426-470 JF https://www.frontiersin.org/articles/10.3389/fgene.2022.1040124/full LK http://dx.doi.org/https://doi.org/10.3389/fgene.2022.1040124 DO https://doi.org/10.3389/fgene.2022.1040124 SF ELIB - SuUB Bremen
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