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Results 1 - 10 of 510 for Van
  1. ... EVC gene have been reported to cause Ellis-van Creveld syndrome, an inherited disorder characterized by dwarfism, ... function underlies the signs and symptoms of Ellis-van Creveld syndrome, researchers believe that it may prevent ...
  2. ... EVC2 gene have been found to cause Ellis-van Creveld syndrome, an inherited disorder characterized by dwarfism, ... function underlies the signs and symptoms of Ellis-van Creveld syndrome, researchers believe that it may prevent ...
  3. ... or Free article on PubMed Central Balemans W, Van Hul W. The genetics of low-density lipoprotein ... B, Sullivan B, Superti-Furga A, Swoboda W, van den Boogaard MJ, Van Hul W, Vikkula M, ...
  4. ... Drop SL, Hermus A, Bocca G, Hoefsloot LH, van Ravenswaaij-Arts CM. The results of CHD7 analysis ... Janssen N, Hoefsloot LH, Jongmans MC, Hofstra RM, van Ravenswaaij-Arts CM. CHD7 mutations and CHARGE syndrome: ...
  5. ... NCBI Gene ClinVar den Hollander AI, Davis J, van der Velde-Visser SD, Zonneveld MN, Pierrottet CO, Koenekoop RK, Kellner U, van den Born LI, Heckenlively JR, Hoyng CB, Handford ...
  6. ... Rodrigues Masruha M, Pereira Vilanova LC, Scheper GC, Van der Knaap MS. Leukoencephalopathy with brainstem and spinal ... 2010 May 25. Citation on PubMed Scheper GC, van der Klok T, van Andel RJ, van Berkel ...
  7. ... 5201189. Citation on PubMed Li W, Wang X, Van Der Knaap MS, Proud CG. Mutations linked to ... 10.1042/BST0331487. Citation on PubMed Pronk JC, van Kollenburg B, Scheper GC, van der Knaap MS. ...
  8. ... DPYD NCBI Gene ClinVar Al-Sanna'a NA, Van Kuilenburg AB, Atrak TM, Abdul-Jabbar MA, Van Gennip AH. Dihydropyrimidine dehydrogenase deficiency presenting at birth. ...
  9. ... Demirdas S, Dulfer E, Robert L, Kempers M, van Beek D, Micha D, van Engelen BG, Hamel B, Schalkwijk J, Loeys B, ... Hendriks AGM, Voermans NC, Schalkwijk J, Hamel BC, van Rossum MM. Well-defined clinical presentation of Ehlers- ...
  10. ... B, Smits AP, Newbury-Ecob R, Hennekam RC, Van Buggenhout G, van Haeringen A, Woods CG, van Essen AJ, de Waal R, Vriend G, Haber DA, Yang A, McKeon F, Brunner HG, van Bokhoven H. Heterozygous germline mutations in the p53 ...
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