van Zandvoort P - Search Results

1

X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism.

Brunner HG, Nelen MR, van Zandvoort P, Abeling NG, van Gennip AH, Wolters EC, Kuiper MA, Ropers HH, van Oost BA. Brunner HG, et al. Among authors: van zandvoort p. Am J Hum Genet. 1993 Jun;52(6):1032-9. Am J Hum Genet. 1993. PMID: 8503438 Free PMC article.

2

Linkage analysis of keratosis follicularis spinulosa decalvans, and regional assignment to human chromosome Xp21.2-p22.2.

Oosterwijk JC, Nelen M, van Zandvoort PM, van Osch LD, Oranje AP, Wittebol-Post D, van Oost BA. Oosterwijk JC, et al. Among authors: van oost ba, van zandvoort pm, van osch ld. Am J Hum Genet. 1992 Apr;50(4):801-7. Am J Hum Genet. 1992. PMID: 1550124 Free PMC article.

3

Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosis.

van Oost BA, van Zandvoort PM, Tünte W, Brunner HG, Hoogeboom AJ, Maaswinkel-Mooy PD, Bakkeren J, Hamel B, Ropers HH. van Oost BA, et al. Among authors: van zandvoort pm. Hum Genet. 1991 Feb;86(4):404-7. doi: 10.1007/BF00201845. Hum Genet. 1991. PMID: 1671851

4

An NcoI restriction fragment length polymorphism at the human steroid sulphatase gene locus.

van Zandvoort PM, van Bennekom CA, Ropers HH, van Oost BA. van Zandvoort PM, et al. Among authors: van oost ba, van bennekom ca. Hum Genet. 1990 Apr;84(5):489-90. doi: 10.1007/BF00195828. Hum Genet. 1990. PMID: 1969847

5

Confirmation of X-linked inheritance and provisional mapping of the keratosis follicularis spinulosa decalvans gene on Xp in a large Dutch family.

Oosterwijk JC, Nelen M, Van Zandvoort PM, Van Osch LD, Oranje AP, Wittebol-Post D, Van Oost BA. Oosterwijk JC, et al. Among authors: van oost ba, van zandvoort pm, van osch ld. Ophthalmic Paediatr Genet. 1992 Mar;13(1):27-30. doi: 10.3109/13816819209070050. Ophthalmic Paediatr Genet. 1992. PMID: 1350668

6

Prenatal exclusion of choroideremia.

van den Hurk JA, van Zandvoort PM, Brunsmann F, Pawlowitzki IH, Holzgreve W, Szabo P, Cremers FP, van Oost BA. van den Hurk JA, et al. Among authors: van oost ba, van zandvoort pm. Am J Med Genet. 1992 Dec 1;44(6):822-3. doi: 10.1002/ajmg.1320440621. Am J Med Genet. 1992. PMID: 1362326

7

NcoI RFLP at the creatine kinase-muscle type gene locus (CKMM, chromosome 19).

Coerwinkel-Driessen M, Schepens J, van Zandvoort P, van Oost B, Mariman E, Wieringa B. Coerwinkel-Driessen M, et al. Among authors: van zandvoort p, van oost b. Nucleic Acids Res. 1988 Sep 12;16(17):8743. doi: 10.1093/nar/16.17.8743. Nucleic Acids Res. 1988. PMID: 2901730 Free PMC article.

8

[Keratosis follicularis spinulosa decalvans (Siemens I syndrome), initial results of molecular genetic research].

Oosterwijk JC, van Osch LD, Wittebol-Post D, Nelen M, van Zandvoort P, Oranje AP, van Oost BA. Oosterwijk JC, et al. Among authors: van oost ba, van zandvoort p, van osch ld. Klin Monbl Augenheilkd. 1992 Dec;201(6):412-3. Klin Monbl Augenheilkd. 1992. PMID: 1287362 German. No abstract available.

9

Linkage analysis by genotyping of sibling populations: a genetic map for the potato cyst nematode constructed using a "pseudo-F2" mapping strategy.

Rouppe van der Voort JN, van Eck HJ, van Zandvoort PM, Overmars H, Helder J, Bakker J. Rouppe van der Voort JN, et al. Among authors: van zandvoort pm. Mol Gen Genet. 1999 Jul;261(6):1021-31. doi: 10.1007/s004380051051. Mol Gen Genet. 1999. PMID: 10485294

10

Effects of 8-aminoguanosine on the toxicity of guanosine and deoxyguanosine for malignant and normal lymphoid cells.

van der Kraan PM, van Zandvoort PM, De Abreu RA, Bakkeren JA. van der Kraan PM, et al. Among authors: van zandvoort pm. J Leukoc Biol. 1988 Jul;44(1):46-50. doi: 10.1002/jlb.44.1.46. J Leukoc Biol. 1988. PMID: 3164750

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