Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2002 | 1 |
2003 | 2 |
2005 | 1 |
2024 | 0 |
Search Results
4 results
Results by year
Filters applied: . Clear all
Page 1
Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15.
Am J Ophthalmol. 2005 Feb;139(2):386-8. doi: 10.1016/j.ajo.2004.08.041.
Am J Ophthalmol. 2005.
PMID: 15734019
Refinement of the physical location and the genomic characterization of the CRSP2 (EXLM1) gene on Xp11.4.
Demirci FY, Ramser J, White NJ, Rigatti BW, Meindl A, Lewis KF, Wen G, Gorin MB.
Demirci FY, et al.
DNA Seq. 2003 Apr;14(2):123-7. doi: 10.1080/1042517021000056952.
DNA Seq. 2003.
PMID: 12825353
Item in Clipboard
A new genetic locus for X linked progressive cone-rod dystrophy.
Jalkanen R, Demirci FY, Tyynismaa H, Bech-Hansen T, Meindl A, Peippo M, Mäntyjärvi M, Gorin MB, Alitalo T.
Jalkanen R, et al.
J Med Genet. 2003 Jun;40(6):418-23. doi: 10.1136/jmg.40.6.418.
J Med Genet. 2003.
PMID: 12807962
Free PMC article.
Item in Clipboard
X-linked recessive atrophic macular degeneration from RPGR mutation.
Ayyagari R, Demirci FY, Liu J, Bingham EL, Stringham H, Kakuk LE, Boehnke M, Gorin MB, Richards JE, Sieving PA.
Ayyagari R, et al.
Genomics. 2002 Aug;80(2):166-71. doi: 10.1006/geno.2002.6815.
Genomics. 2002.
PMID: 12160730
Item in Clipboard
Cite
Cite