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Motor performance in children with Noonan syndrome.
Croonen EA, Essink M, van der Burgt I, Draaisma JM, Noordam C, Nijhuis-van der Sanden MWG. Croonen EA, et al. Among authors: draaisma jm. Am J Med Genet A. 2017 Sep;173(9):2335-2345. doi: 10.1002/ajmg.a.38322. Epub 2017 Jun 19. Am J Med Genet A. 2017. PMID: 28627718
External ear anomalies and hearing impairment in Noonan Syndrome.
van Trier DC, van Nierop J, Draaisma JMT, van der Burgt I, Kunst H, Croonen EA, Admiraal RJC. van Trier DC, et al. Int J Pediatr Otorhinolaryngol. 2015 Jun;79(6):874-878. doi: 10.1016/j.ijporl.2015.03.021. Epub 2015 Apr 1. Int J Pediatr Otorhinolaryngol. 2015. PMID: 25862627
Localization of the ICF syndrome to chromosome 20 by homozygosity mapping.
Wijmenga C, van den Heuvel LP, Strengman E, Luyten JA, van der Burgt IJ, de Groot R, Smeets DF, Draaisma JM, van Dongen JJ, De Abreu RA, Pearson PL, Sandkuijl LA, Weemaes CM. Wijmenga C, et al. Among authors: draaisma jm. Am J Hum Genet. 1998 Sep;63(3):803-9. doi: 10.1086/302021. Am J Hum Genet. 1998. PMID: 9718351 Free PMC article.
133 results