van den Ouweland AM - Search Results

1

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

2

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

3

Colocalization of the gene for nephrogenic diabetes insipidus (DIR) and the vasopressin type 2 receptor gene (AVPR2) in the Xq28 region.

van den Ouweland AM, Knoop MT, Knoers VV, Markslag PW, Rocchi M, Warren ST, Ropers HH, Fahrenholz F, Monnens LA, van Oost BA. van den Ouweland AM, et al. Among authors: van oost ba. Genomics. 1992 Aug;13(4):1350-2. doi: 10.1016/0888-7543(92)90067-3. Genomics. 1992. PMID: 1324225

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

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.

7

DXS539, a polymorphic DNA marker proximal of the fragile-X gene.

Dreesen JC, van den Hurk JA, Smits AP, van den Ouweland AM, Markslag PW, van Oost BA. Dreesen JC, et al. Among authors: van den hurk ja, van oost ba, van den ouweland am. Hum Genet. 1993 Mar;91(1):80-2. doi: 10.1007/BF00230229. Hum Genet. 1993. PMID: 8454292

8

Nephrogenic diabetes insipidus: identification of the genetic defect.

Knoers N, van den Ouweland A, Dreesen J, Verdijk M, Monnens LA, van Oost BA. Knoers N, et al. Pediatr Nephrol. 1993 Oct;7(5):685-8. doi: 10.1007/BF00852579. Pediatr Nephrol. 1993. PMID: 8251344 Review.

9

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

10

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.

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