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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1958 1
1960 1
1961 1
1965 1
1966 1
1967 1
1968 1
1969 2
1970 2
1971 1
1976 1
1977 1
1982 1
1986 1
1987 1
1988 1
1989 1
1990 1
1991 4
1992 1
1993 2
1995 3
1997 1
1998 3
1999 2
2000 2
2002 1
2003 1
2004 1
2005 1
2024 0

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Publication date

PubMed (OMIM) for id: 18145

41 results

Results by year

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Page 1
Dent Disease with mutations in OCRL1.
Hoopes RR Jr, Shrimpton AE, Knohl SJ, Hueber P, Hoppe B, Matyus J, Simckes A, Tasic V, Toenshoff B, Suchy SF, Nussbaum RL, Scheinman SJ. Hoopes RR Jr, et al. Am J Hum Genet. 2005 Feb;76(2):260-7. doi: 10.1086/427887. Epub 2004 Dec 30. Am J Hum Genet. 2005. PMID: 15627218 Free PMC article.
Oculo-cerebral-renal syndrome.
LOWE CU. LOWE CU. Maandschr Kindergeneeskd. 1960 Mar;28:77-80. Maandschr Kindergeneeskd. 1960. PMID: 14418529 No abstract available.
THE OCULO-CEREBRO-RENAL SYNDROME OF LOWE.
RICHARDS W, DONNELL GN, WILSON WA, STOWENS D, PERRY T. RICHARDS W, et al. Am J Dis Child. 1965 Mar;109:185-203. doi: 10.1001/archpedi.1965.02090020187001. Am J Dis Child. 1965. PMID: 14246065 No abstract available.
[Ocular manifestations of Lowe syndrome].
STREIFF EB, STRAUB W, GOLAY L. STREIFF EB, et al. Ophthalmologica. 1958 May-Jun;135(5-6):632-9. doi: 10.1159/000303367. Ophthalmologica. 1958. PMID: 13553275 French. No abstract available.
Unusual renal features of Lowe syndrome in a mildly affected boy.
Gropman A, Levin S, Yao L, Lin T, Suchy S, Sabnis S, Hadley D, Nussbaum R. Gropman A, et al. Am J Med Genet. 2000 Dec 18;95(5):461-6. doi: 10.1002/1096-8628(20001218)95:5<461::aid-ajmg10>3.0.co;2-d. Am J Med Genet. 2000. PMID: 11146467
41 results