Van der Burgt CJ - Search Results

1

Familial Angelman syndrome with a crossover in the critical deletion region.

Nelen MR, Van der Burgt CJ, Nillesen WN, Vis A, Smeets HJ. Nelen MR, et al. Among authors: van der burgt cj. Am J Med Genet. 1994 Sep 1;52(3):352-7. doi: 10.1002/ajmg.1320520320. Am J Med Genet. 1994. PMID: 7810569

2

Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parent.

Van Der Burgt CJ, Merkx GF, Janssen AH, Mulder JC, Suijkerbuijk RF, Smeets DF. Van Der Burgt CJ, et al. J Med Genet. 1992 Oct;29(10):739-41. doi: 10.1136/jmg.29.10.739. J Med Genet. 1992. PMID: 1433237 Free PMC article.

3

Nijmegen Breakage syndrome: a progress report.

Weemaes CM, Smeets DF, van der Burgt CJ. Weemaes CM, et al. Among authors: van der burgt cj. Int J Radiat Biol. 1994 Dec;66(6 Suppl):S185-8. Int J Radiat Biol. 1994. PMID: 7836846 Review.

4

Hearing loss in Noonan syndrome.

Cremers CW, van der Burgt CJ. Cremers CW, et al. Among authors: van der burgt cj. Int J Pediatr Otorhinolaryngol. 1992 Jan;23(1):81-4. doi: 10.1016/0165-5876(92)90082-z. Int J Pediatr Otorhinolaryngol. 1992. PMID: 1592554 Review.

5

A female patient with neurological, facial, digital and renal abnormalities: another case of the neurofaciodigitorenal (NFDR) syndrome?

Rump P, Gruijters MY, Van der Burgt CJ. Rump P, et al. Among authors: van der burgt cj. Clin Dysmorphol. 1997 Oct;6(4):337-40. doi: 10.1097/00019605-199710000-00006. Clin Dysmorphol. 1997. PMID: 9354842

6

Ectrodactyly of lower limbs, congenital heart defect and characteristic facies in four unrelated Dutch patients: a new association.

Van Den Ende JJ, Van Der Burgt CJ, Jansweijer MC, Hamel BC, Brunner HG. Van Den Ende JJ, et al. Among authors: van der burgt cj. Clin Dysmorphol. 1996 Jan;5(1):1-7. doi: 10.1097/00019605-199601000-00001. Clin Dysmorphol. 1996. PMID: 8867653

7

T cell subsets and T cell function in cartilage-hair hypoplasia.

Kooijman R, van der Burgt CJ, Weemaes CM, Haraldsson A, Scholtens EJ, Zegers BJ. Kooijman R, et al. Among authors: van der burgt cj. Scand J Immunol. 1997 Aug;46(2):209-15. doi: 10.1046/j.1365-3083.1997.d01-112.x. Scand J Immunol. 1997. PMID: 9584003 Free article.

8

Myopathology in patients with a Noonan phenotype.

de Boode WP, Semmekrot BA, ter Laak HJ, van der Burgt CJ, Draaisma JM, Lommen EJ, Sengers RC, van Wijk-Hoek JM. de Boode WP, et al. Among authors: van der burgt cj. Acta Neuropathol. 1996 Dec;92(6):597-602. doi: 10.1007/s004010050566. Acta Neuropathol. 1996. PMID: 8960317

9

Antibody deficiency and isolated growth hormone deficiency in a girl with Mulibrey nanism.

Haraldsson A, van der Burgt CJ, Weemaes CM, Otten B, Bakkeren JA, Stoelinga GB. Haraldsson A, et al. Among authors: van der burgt cj. Eur J Pediatr. 1993 Jun;152(6):509-12. doi: 10.1007/BF01955061. Eur J Pediatr. 1993. PMID: 8335020

10

[The Noonan syndrome from a pediatric perspective].

Noordam C, Thoonen G, van der Burgt CJ. Noordam C, et al. Among authors: van der burgt cj. Ned Tijdschr Geneeskd. 2003 Apr 5;147(14):644-8. Ned Tijdschr Geneeskd. 2003. PMID: 12712646 Review. Dutch.

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