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 |
---|---|
1990 | 1 |
1996 | 1 |
1997 | 1 |
2024 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
Page 1
Microphthalmos in the presumed homozygous offspring of a first cousin marriage and linkage analysis of a locus in a family with autosomal dominant cerulean congenital cataracts.
Am J Med Genet. 1990 Sep;37(1):54-9. doi: 10.1002/ajmg.1320370113.
Am J Med Genet. 1990.
PMID: 2240043
Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2.
Litt M, Carrero-Valenzuela R, LaMorticella DM, Schultz DW, Mitchell TN, Kramer P, Maumenee IH.
Litt M, et al.
Hum Mol Genet. 1997 May;6(5):665-8. doi: 10.1093/hmg/6.5.665.
Hum Mol Genet. 1997.
PMID: 9158139
Item in Clipboard
A second gene for cerulean cataracts maps to the beta crystallin region on chromosome 22.
Kramer P, Yount J, Mitchell T, LaMorticella D, Carrero-Valenzuela R, Lovrien E, Maumenee I, Litt M.
Kramer P, et al.
Genomics. 1996 Aug 1;35(3):539-42. doi: 10.1006/geno.1996.0395.
Genomics. 1996.
PMID: 8812489
Free article.
Item in Clipboard
Cite
Cite