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3-M syndrome: description of six new patients with review of the literature.
van der Wal G, Otten BJ, Brunner HG, van der Burgt I. van der Wal G, et al. Among authors: van der burgt i. Clin Dysmorphol. 2001 Oct;10(4):241-52. doi: 10.1097/00019605-200110000-00002. Clin Dysmorphol. 2001. PMID: 11665997 Review.
Cartilage hair hypoplasia, metaphyseal chondrodysplasia type McKusick: description of seven patients and review of the literature.
van der Burgt I, Haraldsson A, Oosterwijk JC, van Essen AJ, Weemaes C, Hamel B. van der Burgt I, et al. Among authors: van essen aj. Am J Med Genet. 1991 Dec 1;41(3):371-80. doi: 10.1002/ajmg.1320410320. Am J Med Genet. 1991. PMID: 1789294 Review.
Further delineation of the branchio-oculo-facial syndrome.
Lin AE, Gorlin RJ, Lurie IW, Brunner HG, van der Burgt I, Naumchik IV, Rumyantseva NV, Stengel-Rutkowski S, Rosenbaum K, Meinecke P, et al. Lin AE, et al. Among authors: van der burgt i. Am J Med Genet. 1995 Mar 13;56(1):42-59. doi: 10.1002/ajmg.1320560112. Am J Med Genet. 1995. PMID: 7747785 Review.
Clinical and molecular studies in a large Dutch family with Noonan syndrome.
van der Burgt I, Berends E, Lommen E, van Beersum S, Hamel B, Mariman E. van der Burgt I, et al. Among authors: van beersum s. Am J Med Genet. 1994 Nov 1;53(2):187-91. doi: 10.1002/ajmg.1320530213. Am J Med Genet. 1994. PMID: 7856646
Xeroderma pigmentosum--Cockayne syndrome complex: a further case.
Hamel BC, Raams A, Schuitema-Dijkstra AR, Simons P, van der Burgt I, Jaspers NG, Kleijer WJ. Hamel BC, et al. Among authors: van der burgt i. J Med Genet. 1996 Jul;33(7):607-10. doi: 10.1136/jmg.33.7.607. J Med Genet. 1996. PMID: 8818951 Free PMC article.
Nijmegen breakage syndrome.
van der Burgt I, Chrzanowska KH, Smeets D, Weemaes C. van der Burgt I, et al. J Med Genet. 1996 Feb;33(2):153-6. doi: 10.1136/jmg.33.2.153. J Med Genet. 1996. PMID: 8929954 Free PMC article. Review.
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: van den heuvel lp, van der burgt ij, van dongen jj. Am J Hum Genet. 1998 Sep;63(3):803-9. doi: 10.1086/302021. Am J Hum Genet. 1998. PMID: 9718351 Free PMC article.
Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expression.
van der Burgt I, Thoonen G, Roosenboom N, Assman-Hulsmans C, Gabreels F, Otten B, Brunner HG. van der Burgt I, et al. J Pediatr. 1999 Dec;135(6):707-13. doi: 10.1016/s0022-3476(99)70089-2. J Pediatr. 1999. PMID: 10586173
Genetic heterogeneity in Noonan syndrome: evidence for an autosomal recessive form.
van Der Burgt I, Brunner H. van Der Burgt I, et al. Am J Med Genet. 2000 Sep 4;94(1):46-51. doi: 10.1002/1096-8628(20000904)94:1<46::aid-ajmg10>3.0.co;2-i. Am J Med Genet. 2000. PMID: 10982482
Growth hormone (GH) secretion in children with Noonan syndrome: frequently abnormal without consequences for growth or response to GH treatment.
Noordam C, van der Burgt I, Sweep CG, Delemarre-van de Waal HA, Sengers RC, Otten BJ. Noordam C, et al. Among authors: van der burgt i. Clin Endocrinol (Oxf). 2001 Jan;54(1):53-9. doi: 10.1046/j.1365-2265.2001.01188.x. Clin Endocrinol (Oxf). 2001. PMID: 11167926
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