van Oost BA - Search Results

1

Nephrogenic diabetes insipidus: close linkage with markers from the distal long arm of the human X chromosome.

Knoers N, van der Heyden H, van Oost BA, Ropers HH, Monnens L, Willems J. Knoers N, et al. Among authors: van oost ba, van der heyden h. Hum Genet. 1988 Sep;80(1):31-8. doi: 10.1007/BF00451451. Hum Genet. 1988. PMID: 2843456

2

Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutation.

Traupe H, Müller D, Atherton D, Kalter DC, Cremers FP, van Oost BA, Ropers HH. Traupe H, et al. Among authors: van oost ba. Hum Genet. 1992 Aug;89(6):659-65. doi: 10.1007/BF00221958. Hum Genet. 1992. PMID: 1355069

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

Linkage analyses in families with nephrogenic diabetes insipidus.

Knoers NV, van der Heyden H, van Oost BA, Monnens L, Willems J, Ropers HH. Knoers NV, et al. Among authors: van oost ba, van der heyden h. Prog Clin Biol Res. 1989;305:149-55. Prog Clin Biol Res. 1989. PMID: 2569742 No abstract available.

6

Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM).

Brunner HG, Korneluk RG, Coerwinkel-Driessen M, MacKenzie A, Smeets H, Lambermon HM, van Oost BA, Wieringa B, Ropers HH. Brunner HG, et al. Among authors: van oost ba. Hum Genet. 1989 Mar;81(4):308-10. doi: 10.1007/BF00283680. Hum Genet. 1989. PMID: 2703233

7

Three-point linkage analysis using multiple DNA polymorphic markers in families with X-linked nephrogenic diabetes insipidus.

Knoers N, van der Heyden H, van Oost BA, Monnens L, Willems J, Ropers HH. Knoers N, et al. Among authors: van oost ba, van der heyden h. Genomics. 1989 Apr;4(3):434-7. doi: 10.1016/0888-7543(89)90352-2. Genomics. 1989. PMID: 2714800

8

Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene.

van Lieburg AF, Verdijk MA, Knoers VV, van Essen AJ, Proesmans W, Mallmann R, Monnens LA, van Oost BA, van Os CH, Deen PM. van Lieburg AF, et al. Among authors: van essen aj, van os ch, van oost ba. Am J Hum Genet. 1994 Oct;55(4):648-52. Am J Hum Genet. 1994. PMID: 7524315 Free PMC article.

9

Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutation.

van Lieburg AF, Verdijk MA, Schoute F, Ligtenberg MJ, van Oost BA, Waldhauser F, Dobner M, Monnens LA, Knoers NV. van Lieburg AF, et al. Among authors: van oost ba. Hum Genet. 1995 Jul;96(1):70-8. doi: 10.1007/BF00214189. Hum Genet. 1995. PMID: 7607658 Free article. Review.

10

The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region.

Wijker M, Ligtenberg MJ, Schoute F, Defesche JC, Pals G, Bolhuis PA, Ropers HH, Hulsebos TJ, Menko FH, van Oost BA, et al. Wijker M, et al. Among authors: van oost ba. Am J Hum Genet. 1995 May;56(5):1096-100. Am J Hum Genet. 1995. PMID: 7726164 Free PMC article.

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