van Oost BA - Search Results

1

Identification and characterization of a new gene in the human Xq28 region.

van den Ouweland AM, Kioschis P, Verdijk M, Tamanini F, Toniolo D, Poustka A, van Oost BA. van den Ouweland AM, et al. Among authors: van oost ba. Hum Mol Genet. 1992 Jul;1(4):269-73. doi: 10.1093/hmg/1.4.269. Hum Mol Genet. 1992. PMID: 1303197

2

The human renin-binding protein gene (RENBP) maps in Xq28.

van den Ouweland AM, Verdijk M, Kiochis P, Poustka A, van Oost BA. van den Ouweland AM, et al. Among authors: van oost ba. Genomics. 1994 May 1;21(1):279-81. doi: 10.1006/geno.1994.1259. Genomics. 1994. PMID: 8088804 No abstract available.

3

Mutations in the vasopressin type 2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidus.

van den Ouweland AM, Dreesen JC, Verdijk M, Knoers NV, Monnens LA, Rocchi M, van Oost BA. van den Ouweland AM, et al. Among authors: van oost ba. Nat Genet. 1992 Oct;2(2):99-102. doi: 10.1038/ng1092-99. Nat Genet. 1992. PMID: 1303271

4

The QM gene is X-linked and therefore not involved in suppression of tumorigenesis in Wilms' tumor.

van den Ouweland AM, Verdijk M, Mannens MM, van Oost BA. van den Ouweland AM, et al. Among authors: van oost ba. Hum Genet. 1992 Sep-Oct;90(1-2):144-6. doi: 10.1007/BF00210759. Hum Genet. 1992. PMID: 1330878

5

Validation of linkage-based DNA-diagnosis of fragile X gene carriers with the CGG repeat probe.

van Oost BA, Smits AP, Dreesen JC, van den Ouweland AM, Oostra BA. van Oost BA, et al. Among authors: van den ouweland am. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):320-7. doi: 10.1002/ajmg.1320430149. Am J Med Genet. 1992. PMID: 1605205

6

Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panel.

Traupe H, van den Ouweland AM, van Oost BA, Vogel W, Vetter U, Warren ST, Rocchi M, Darlison MG, Ropers HH. Traupe H, et al. Among authors: van oost ba, van den ouweland am. Genomics. 1992 Jun;13(2):481-3. doi: 10.1016/0888-7543(92)90279-2. Genomics. 1992. PMID: 1612609

7

Two polymorphisms at the DXS539 locus.

van den Hurk JA, Dreesen JC, van den Berg H, van Bennekom CA, van den Ouweland AM, van Oost BA. van den Hurk JA, et al. Among authors: van oost ba, van den berg h, van den ouweland am, van bennekom ca. Nucleic Acids Res. 1991 Apr 11;19(7):1723. doi: 10.1093/nar/19.7.1723. Nucleic Acids Res. 1991. PMID: 1674141 Free PMC article. No abstract available.

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

Inheritance of mutations in the V2 receptor gene in thirteen families with nephrogenic diabetes insipidus.

Knoers NV, van den Ouweland AM, Verdijk M, Monnens LA, van Oost BA. Knoers NV, et al. Among authors: van oost ba, van den ouweland am. Kidney Int. 1994 Jul;46(1):170-6. doi: 10.1038/ki.1994.256. Kidney Int. 1994. PMID: 7933835 Free article.

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