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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1992 | 1 |
1995 | 1 |
1997 | 1 |
2004 | 1 |
2006 | 1 |
2010 | 1 |
2024 | 0 |
PubMed (cited) for id: 123631
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Page 1
A missense mutation in CRYBA4 associated with congenital cataract and microcornea.
Mol Vis. 2010 Jun 5;16:1019-24.
Mol Vis. 2010.
PMID: 20577656
Free PMC article.
CRYBA4, a novel human cataract gene, is also involved in microphthalmia.
Billingsley G, Santhiya ST, Paterson AD, Ogata K, Wodak S, Hosseini SM, Manisastry SM, Vijayalakshmi P, Gopinath PM, Graw J, Héon E.
Billingsley G, et al.
Am J Hum Genet. 2006 Oct;79(4):702-9. doi: 10.1086/507712. Epub 2006 Aug 17.
Am J Hum Genet. 2006.
PMID: 16960806
Free PMC article.
Item in Clipboard
Mutation analysis of congenital cataracts in Indian families: identification of SNPS and a new causative allele in CRYBB2 gene.
Santhiya ST, Manisastry SM, Rawlley D, Malathi R, Anishetty S, Gopinath PM, Vijayalakshmi P, Namperumalsamy P, Adamski J, Graw J.
Santhiya ST, et al.
Invest Ophthalmol Vis Sci. 2004 Oct;45(10):3599-607. doi: 10.1167/iovs.04-0207.
Invest Ophthalmol Vis Sci. 2004.
PMID: 15452067
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Sequence analysis of betaA3, betaB3, and betaA4 crystallins completes the identification of the major proteins in young human lens.
Lampi KJ, Ma Z, Shih M, Shearer TR, Smith JB, Smith DL, David LL.
Lampi KJ, et al.
J Biol Chem. 1997 Jan 24;272(4):2268-75. doi: 10.1074/jbc.272.4.2268.
J Biol Chem. 1997.
PMID: 8999933
Free article.
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The beta crystallin genes on human chromosome 22 define a new region of homology with mouse chromosome 5.
Hulsebos TJ, Jenkins NA, Gilbert DJ, Copeland NG.
Hulsebos TJ, et al.
Genomics. 1995 Jan 20;25(2):574-6. doi: 10.1016/0888-7543(95)80062-q.
Genomics. 1995.
PMID: 7789995
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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.
Cytogenet Cell Genet. 1992;61(3):180-3. doi: 10.1159/000133403.
Cytogenet Cell Genet. 1992.
PMID: 1424806
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