Similar articles for PMID: 2798422

Year	Number of Results
1951	1
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1987	6
1988	2
1989	5
1990	9
1991	5
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1994	3
1995	4
1996	3
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1998	3
1999	2
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2003	1
2005	1
2009	1
2015	2
2017	1
2019	1
2024	0

1

Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia.

Cremers FP, van de Pol DJ, Wieringa B, Collins FS, Sankila EM, Siu VM, Flintoff WF, Brunsmann F, Blonden LA, Ropers HH. Cremers FP, et al. Proc Natl Acad Sci U S A. 1989 Oct;86(19):7510-4. doi: 10.1073/pnas.86.19.7510. Proc Natl Acad Sci U S A. 1989. PMID: 2798422 Free PMC article.

2

Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases.

Cremers FP, Sankila EM, Brunsmann F, Jay M, Jay B, Wright A, Pinckers AJ, Schwartz M, van de Pol DJ, Wieringa B, et al. Cremers FP, et al. Am J Hum Genet. 1990 Oct;47(4):622-8. Am J Hum Genet. 1990. PMID: 2220804 Free PMC article.

3

DXS165 detects a translocation breakpoint in a woman with choroideremia and a de novo X; 13 translocation.

Merry DE, Lesko JG, Siu V, Flintoff WF, Collins F, Lewis RA, Nussbaum RL. Merry DE, et al. Genomics. 1990 Apr;6(4):609-15. doi: 10.1016/0888-7543(90)90494-f. Genomics. 1990. PMID: 2341150 Free article.

4

Deletion of the DXS165 locus in patients with classical choroideremia.

Cremers FP, Brunsmann F, van de Pol TJ, Pawlowitzki IH, Paulsen K, Wieringa B, Ropers HH. Cremers FP, et al. Clin Genet. 1987 Dec;32(6):421-3. doi: 10.1111/j.1399-0004.1987.tb03166.x. Clin Genet. 1987. PMID: 3481306

5

Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21.

Merry DE, Lesko JG, Sosnoski DM, Lewis RA, Lubinsky M, Trask B, van den Engh G, Collins FS, Nussbaum RL. Merry DE, et al. Am J Hum Genet. 1989 Oct;45(4):530-40. Am J Hum Genet. 1989. PMID: 2491012 Free PMC article.

6

Cloning of a gene that is rearranged in patients with choroideraemia.

Cremers FP, van de Pol DJ, van Kerkhoff LP, Wieringa B, Ropers HH. Cremers FP, et al. Nature. 1990 Oct 18;347(6294):674-7. doi: 10.1038/347674a0. Nature. 1990. PMID: 2215697

7

DXS26 (HU16) is located in Xq21.1.

Sankila EM, Bruns GA, Schwartz M, Nikoskelainen E, Niebuhr E, Hodgson SV, Wright AF, de la Chapelle A. Sankila EM, et al. Hum Genet. 1990 Jun;85(1):117-20. doi: 10.1007/BF00276335. Hum Genet. 1990. PMID: 2162804

8

Linkage studies and deletion screening in choroideremia.

Wright AF, Nussbaum RL, Bhattacharya SS, Jay M, Lesko JG, Evans HJ, Jay B. Wright AF, et al. J Med Genet. 1990 Aug;27(8):496-8. doi: 10.1136/jmg.27.8.496. J Med Genet. 1990. PMID: 1976814 Free PMC article.

9

Choroideremia associated with an X-autosomal translocation.

Siu VM, Gonder JR, Jung JH, Sergovich FR, Flintoff WF. Siu VM, et al. Hum Genet. 1990 Apr;84(5):459-64. doi: 10.1007/BF00195820. Hum Genet. 1990. PMID: 2323779 Free PMC article.

10

Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes.

Cremers FP, van de Pol DJ, Diergaarde PJ, Wieringa B, Nussbaum RL, Schwartz M, Ropers HH. Cremers FP, et al. Genomics. 1989 Jan;4(1):41-6. doi: 10.1016/0888-7543(89)90312-1. Genomics. 1989. PMID: 2914708

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