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2. The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families. Fountain MD; Aten E; Cho MT; Juusola J; Walkiewicz MA; Ray JW; Xia F; Yang Y; Graham BH; Bacino CA; Potocki L; van Haeringen A; Ruivenkamp CA; Mancias P; Northrup H; Kukolich MK; Weiss MM; van Ravenswaaij-Arts CM; Mathijssen IB; Levesque S; Meeks N; Rosenfeld JA; Lemke D; Hamosh A; Lewis SK; Race S; Stewart LL; Hay B; Lewis AM; Guerreiro RL; Bras JT; Martins MP; Derksen-Lubsen G; Peeters E; Stumpel C; Stegmann S; Bok LA; Santen GW; Schaaf CP Genet Med; 2017 Jan; 19(1):45-52. PubMed ID: 27195816 [TBL] [Abstract][Full Text] [Related]
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8. Diagnosis of Schaaf-Yang syndrome in Korean children with developmental delay and hypotonia. Ahn H; Seo GH; Oh A; Lee Y; Keum C; Heo SH; Kim T; Choi J; Kim GH; Ko TS; Yum MS; Lee BH; Choi IH Medicine (Baltimore); 2020 Dec; 99(51):e23864. PubMed ID: 33371171 [TBL] [Abstract][Full Text] [Related]
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16. Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy. Negishi Y; Ieda D; Hori I; Nozaki Y; Yamagata T; Komaki H; Tohyama J; Nagasaki K; Tada H; Saitoh S Orphanet J Rare Dis; 2019 Dec; 14(1):277. PubMed ID: 31791363 [TBL] [Abstract][Full Text] [Related]
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