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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1994 | 1 |
1995 | 1 |
1997 | 1 |
2024 | 0 |
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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
Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome.
Lugenbeel KA, Peier AM, Carson NL, Chudley AE, Nelson DL.
Lugenbeel KA, et al.
Nat Genet. 1995 Aug;10(4):483-5. doi: 10.1038/ng0895-483.
Nat Genet. 1995.
PMID: 7670500
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Isolation and chromosomal mapping of genomic clones encoding the human fatty acid synthase gene.
Jayakumar A, Chirala SS, Chinault AC, Baldini A, Abu-Elheiga L, Wakil SJ.
Jayakumar A, et al.
Genomics. 1994 Sep 15;23(2):420-4. doi: 10.1006/geno.1994.1518.
Genomics. 1994.
PMID: 7835891
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