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[Prader-Labhart-Willi syndrome in infants].
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
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9 Mb deletion including chromosome band 3q24 associated with unsuspicious facial gestalt, persistent ductus omphaloentericus, mild mental retardation and tic.
Zweier C, Guth S, Schulte-Mattler U, Rauch A, Trautmann U.
Zweier C, et al. Among authors: schulte mattler u.
Eur J Med Genet. 2005 Jul-Sep;48(3):360-2. doi: 10.1016/j.ejmg.2005.04.016.
Eur J Med Genet. 2005.
PMID: 16179233
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