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2002 1
2005 1
2016 1
2017 1
2021 0
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[Prader-Labhart-Willi syndrome in infants].
Schmeling H, Gillessen-Kaesbach G, Schulte-Mattler U, Burdach S, Horneff G. Schmeling H, et al. Among authors: schulte mattler u. Klin Padiatr. 2002 Mar-Apr;214(2):51-3. doi: 10.1055/s-2002-25265. Klin Padiatr. 2002. PMID: 11972309 German.
FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum.
Reuter MS, Riess A, Moog U, Briggs TA, Chandler KE, Rauch A, Stampfer M, Steindl K, Gläser D, Joset P; DDD Study, Krumbiegel M, Rabe H, Schulte-Mattler U, Bauer P, Beck-Wödl S, Kohlhase J, Reis A, Zweier C. Reuter MS, et al. Among authors: schulte mattler u. J Med Genet. 2017 Jan;54(1):64-72. doi: 10.1136/jmedgenet-2016-104094. Epub 2016 Aug 29. J Med Genet. 2017. PMID: 27572252