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Results 1 - 10 of 11 for "Schuurs-hoeijmakers" syndrome
  1. ... disability-craniofacial dysmorphism-cryptorchidism syndrome PACS1-related syndrome Schuurs-Hoeijmakers syndrome SHMS Genetic Testing Registry: Schuurs-hoeijmakers syndrome Intellectual ...
  2. ... Disorders (NORD) ClinicalTrials.gov CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB PubMed Bijlsma EK, Gijsbers AC, Schuurs-Hoeijmakers JH, van Haeringen A, Fransen van de Putte ...
  3. ... Oud MM, Bolat E, Spruijt L, Cornelissen EA, Schuurs-Hoeijmakers JH, de Leeuw N, Cormier-Daire V, Brunner HG, Knoers NV, Roepman R. C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome. J Med Genet. 2011 Jun;48(6):390- ...
  4. ... 37476. Epub 2016 Feb 3. Citation on PubMed ... recognizable intellectual-disability syndrome. Am J Hum Genet. 2012 Dec 7;91( ...
  5. ... Vandeweyer G, Rooms L, van den Ende J, Schuurs-Hoeijmakers JH, Marcelis CL, ... SWI/SNF-related autism syndrome caused by de novo mutations in ADNP. Nat ...
  6. ... Vandeweyer G, Rooms L, van den Ende J, Schuurs-Hoeijmakers JH, Marcelis CL, ... SWI/SNF-related autism syndrome caused by de novo mutations in ADNP. Nat ...
  7. ... Brunner HG, van der Burgt I, Ockeloen CW, Schuurs-Hoeijmakers JH, Klein Wassink-Ruiter JS, Stumpel C, Stevens ...
  8. ... Vaz FM, Gardeitchik T, Vissers LE, Renkema GH, Schuurs-Hoeijmakers JH, Kulik W, Lammens M, Christin C, Kluijtmans ...
  9. ... Vaz FM, Gardeitchik T, Vissers LE, Renkema GH, Schuurs-Hoeijmakers JH, Kulik W, Lammens M, Christin C, Kluijtmans ...
  10. ... Brunner HG, van der Burgt I, Ockeloen CW, Schuurs-Hoeijmakers JH, Klein Wassink-Ruiter JS, Stumpel C, Stevens ...
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