All individuals with variants in gene SHOC2

8 entries on 1 page. Showing entries 1 - 8.
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00080913 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - NSLH1 Noonan-like syndrome with loose anagen hair (OMIM:607721) 1 1 Daniel Trujillano
00228780 17-1777 - - M no Albania - 01y - - - NSLH1 Noonan syndrome like disorder with loose anagen hair 1 1 Paola Daniele
00306134 68 - - F - China - - - - - NSLH1 - 1 1 Sha Hong
00307813 UK10K_FINDWGA5411252 PubMed: Grozeva 2015, Journal: Grozeva 2015 - M - - - - - - - ID - 1 1 Johan den Dunnen
00410431 Patient 6 - - F no China - - - - - NSLH1 - 1 1 Simin Zheng
00419542 9106 PubMed: Marinakis 2021 - F - Greece - - - - - ? - 1 1 Jan Traeger-Synodinos
00440367 PED2066.1 PubMed: Nambot 2018 - - - France - - - - - ? - 1 1 Johan den Dunnen
00467761 Pat18 PubMed: Erkut 2025, Journal: Erkut 2025 2-generation family, 1 affected, unaffected non-carrier parents M - - - - - - - NDD see paper; ..., ventricular septal defect, right-sided aortic arch, vascular ring; acrocephaly, downslanting palpebral fissures, epicanthal folds, telecanthus, deeply set eyes, maxillary hypoplasia, malar hypoplasia, micrognathia, triangular facies, asymmetry, tented lips, high arched palate, small flat teeth; developmental delay; no seizures; father downslanting palpebral fissures 1 1 Johan den Dunnen
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