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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1992 | 1 |
1994 | 1 |
1997 | 2 |
2024 | 0 |
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Page 1
Physical mapping and genomic structure of the Lowe syndrome gene OCRL1.
Hum Genet. 1997 Feb;99(2):145-50. doi: 10.1007/s004390050329.
Hum Genet. 1997.
PMID: 9048911
Localization of the 75-kDa inositol polyphosphate-5-phosphatase (INPP5B) to human chromosome band 1p34.
Jänne PA, Dutra AS, Dracopoli NC, Charnas LR, Puck JM, Nussbaum RL.
Jänne PA, et al.
Cytogenet Cell Genet. 1994;66(3):164-6. doi: 10.1159/000133691.
Cytogenet Cell Genet. 1994.
PMID: 8125013
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Construction and characterization of a yeast artificial chromosome library for Xpter-Xq27.3: a systematic determination of cocloning rate and X-chromosome representation.
Lee JT, Murgia A, Sosnoski DM, Olivos IM, Nussbaum RL.
Lee JT, et al.
Genomics. 1992 Mar;12(3):526-33. doi: 10.1016/0888-7543(92)90444-w.
Genomics. 1992.
PMID: 1559703
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Spectrum of mutations in the OCRL1 gene in the Lowe oculocerebrorenal syndrome.
Lin T, Orrison BM, Leahey AM, Suchy SF, Bernard DJ, Lewis RA, Nussbaum RL.
Lin T, et al.
Am J Hum Genet. 1997 Jun;60(6):1384-8. doi: 10.1086/515471.
Am J Hum Genet. 1997.
PMID: 9199559
Free PMC article.
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