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

Year Number of Results
1994 1
1999 7
2000 3
2001 2
2002 3
2003 1
2004 2
2005 3
2006 2
2008 2
2010 1
2013 4
2014 2
2018 1
2023 0

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Page 1
Leber congenital amaurosis.
Perrault I, Rozet JM, Gerber S, Ghazi I, Leowski C, Ducroq D, Souied E, Dufier JL, Munnich A, Kaplan J. Perrault I, et al. Among authors: ducroq d. Mol Genet Metab. 1999 Oct;68(2):200-8. doi: 10.1006/mgme.1999.2906. Mol Genet Metab. 1999. PMID: 10527670 Review.
[Hereditary macular dystrophies].
Rozet JM, Gerber S, Ducroq D, Hamel C, Dufier JL, Kaplan J. Rozet JM, et al. Among authors: ducroq d. J Fr Ophtalmol. 2005 Jan;28(1):113-24. doi: 10.1016/s0181-5512(05)81033-2. J Fr Ophtalmol. 2005. PMID: 15767907 Review. French.
Spectrum of retGC1 mutations in Leber's congenital amaurosis.
Perrault I, Rozet JM, Gerber S, Ghazi I, Ducroq D, Souied E, Leowski C, Bonnemaison M, Dufier JL, Munnich A, Kaplan J. Perrault I, et al. Among authors: ducroq d. Eur J Hum Genet. 2000 Aug;8(8):578-82. doi: 10.1038/sj.ejhg.5200503. Eur J Hum Genet. 2000. PMID: 10951519
The ABCA4 gene in autosomal recessive cone-rod dystrophies.
Ducroq D, Rozet JM, Gerber S, Perrault I, Barbet D, Hanein S, Hakiki S, Dufier JL, Munnich A, Hamel C, Kaplan J. Ducroq D, et al. Am J Hum Genet. 2002 Dec;71(6):1480-2. doi: 10.1086/344829. Am J Hum Genet. 2002. PMID: 12515255 Free PMC article. No abstract available.
A third locus for dominant optic atrophy on chromosome 22q.
Barbet F, Hakiki S, Orssaud C, Gerber S, Perrault I, Hanein S, Ducroq D, Dufier JL, Munnich A, Kaplan J, Rozet JM. Barbet F, et al. Among authors: ducroq d. J Med Genet. 2005 Jan;42(1):e1. doi: 10.1136/jmg.2004.025502. J Med Genet. 2005. PMID: 15635063 Free PMC article. No abstract available.
32 results