van Oost BA - Search Results

1

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

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

A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19.

Brunner HG, Smeets H, Lambermon HM, Coerwinkel-Driessen M, van Oost BA, Wieringa B, Ropers HH. Brunner HG, et al. Among authors: van oost ba. Genomics. 1989 Oct;5(3):589-95. doi: 10.1016/0888-7543(89)90027-x. Genomics. 1989. PMID: 2575588

4

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

5

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.

6

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

7

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

8

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.

9

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

10

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

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