Geurts van Kessel AH - Search Results

1

An autosomal homologue of the choroideremia gene colocalizes with the Usher syndrome type II locus on the distal part of chromosome 1q.

Cremers FP, Molloy CM, van de Pol DJ, van den Hurk JA, Bach I, Geurts van Kessel AH, Ropers HH. Cremers FP, et al. Among authors: geurts van kessel ah. Hum Mol Genet. 1992 May;1(2):71-5. doi: 10.1093/hmg/1.2.71. Hum Mol Genet. 1992. PMID: 1301160

2

Molecular cloning of the synovial sarcoma-specific translocation (X;18)(p11.2;q11.2) breakpoint.

de Leeuw B, Balemans M, Weghuis DO, Seruca R, Janz M, Geraghty MT, Gilgenkrantz S, Ropers HH, Geurts van Kessel A. de Leeuw B, et al. Hum Mol Genet. 1994 May;3(5):745-9. doi: 10.1093/hmg/3.5.745. Hum Mol Genet. 1994. PMID: 8081361

3

Generation and characterization of radiation reduced cell hybrids and isolation of probes from the proximal short arm of the human X chromosome.

Berger W, Meindl A, de Leeuw B, de Roos A, van de Pol TJ, Meitinger T, van der Velde-Visser SD, Achatz H, Geurts van Kessel A, Cremers FP, et al. Berger W, et al. Hum Genet. 1992 Nov;90(3):243-6. doi: 10.1007/BF00220070. Hum Genet. 1992. PMID: 1487237

4

Mapping of the choroideremia-like (CHML) gene at 1q42-qter and mutation analysis in patients with Usher syndrome type II.

von Bokhoven H, von Genderen C, Molloy CM, van de Pol DJ, Cremers CW, von Aarem A, Schwartz M, Rosenberg T, Geurts van Kessel AH, Ropers HH, et al. von Bokhoven H, et al. Among authors: geurts van kessel ah. Genomics. 1994 Jan 15;19(2):385-7. doi: 10.1006/geno.1994.1077. Genomics. 1994. PMID: 8188272

5

Localization of the cellular retinoic acid binding protein (CRABP) gene relative to the acute promyelocytic leukemia-associated breakpoint on human chromosome 15.

Geurts van Kessel A, de Leeuw H, Dekker EJ, Rijks L, Spurr N, Ledbetter D, Kootwijk E, Vaessen MJ. Geurts van Kessel A, et al. Hum Genet. 1991 Jun;87(2):201-4. doi: 10.1007/BF00204182. Hum Genet. 1991. PMID: 1648546 Free article.

6

Assignment of the gene(s) involved in the expression of the proliferation-related Ki-67 antigen to human chromosome 10.

Schonk DM, Kuijpers HJ, van Drunen E, van Dalen CH, Geurts van Kessel AH, Verheijen R, Ramaekers FC. Schonk DM, et al. Among authors: van drunen e, geurts van kessel ah, van dalen ch. Hum Genet. 1989 Oct;83(3):297-9. doi: 10.1007/BF00285178. Hum Genet. 1989. PMID: 2571566

7

Identification of two alternative fusion genes, SYT-SSX1 and SYT-SSX2, in t(X;18)(p11.2;q11.2)-positive synovial sarcomas.

de Leeuw B, Balemans M, Olde Weghuis D, Geurts van Kessel A. de Leeuw B, et al. Hum Mol Genet. 1995 Jun;4(6):1097-9. doi: 10.1093/hmg/4.6.1097. Hum Mol Genet. 1995. PMID: 7655467 No abstract available.

8

Fine mapping of the 1q21 breakpoint of the papillary renal cell carcinoma-associated (X;1) translocation.

Weterman MA, Wilbrink M, Dijkhuizen T, van den Berg E, Geurts van Kessel A. Weterman MA, et al. Hum Genet. 1996 Jul;98(1):16-21. doi: 10.1007/s004390050153. Hum Genet. 1996. PMID: 8682500 Free article.

9

Demonstration of the genuine iso-12p character of the standard marker chromosome of testicular germ cell tumors and identification of further chromosome 12 aberrations by competitive in situ hybridization.

Suijkerbuijk RF, van de Veen AY, van Echten J, Buys CH, de Jong B, Oosterhuis JW, Warburton DA, Cassiman JJ, Schonk D, Geurts van Kessel A. Suijkerbuijk RF, et al. Am J Hum Genet. 1991 Feb;48(2):269-73. Am J Hum Genet. 1991. PMID: 1846721 Free PMC article.

10

Localization of the beta A4-crystallin gene (CRYBA4) on human chromosome 22 in the region q11.2-->q13.1.

van Rens GL, Geurts van Kessel AH, Bloemendal H. van Rens GL, et al. Among authors: geurts van kessel ah. Cytogenet Cell Genet. 1992;61(3):180-3. doi: 10.1159/000133403. Cytogenet Cell Genet. 1992. PMID: 1424806

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