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

Year Number of Results
1992 3
1993 2
1994 1
1996 2
1999 1
2001 1
2006 2
2007 2
2009 3
2022 0
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17 results
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Page 1
Genetic heterogeneity of familial hemiplegic migraine.
Joutel A, Ducros A, Vahedi K, Labauge P, Delrieu O, Pinsard N, Mancini J, Ponsot G, Gouttière F, Gastaut JL, et al. Joutel A, et al. Among authors: delrieu o. Am J Hum Genet. 1994 Dec;55(6):1166-72. Am J Hum Genet. 1994. PMID: 7977376 Free PMC article.
Phenotype-genotype correlations in X linked retinitis pigmentosa.
Kaplan J, Pelet A, Martin C, Delrieu O, Aymé S, Bonneau D, Briard ML, Hanauer A, Larget-Piet L, Lefrançois P, et al. Kaplan J, et al. Among authors: delrieu o. J Med Genet. 1992 Sep;29(9):615-23. doi: 10.1136/jmg.29.9.615. J Med Genet. 1992. PMID: 1357178 Free PMC article.
A gene for Usher syndrome type I (USH1A) maps to chromosome 14q.
Kaplan J, Gerber S, Bonneau D, Rozet JM, Delrieu O, Briard ML, Dollfus H, Ghazi I, Dufier JL, Frézal J, et al. Kaplan J, et al. Among authors: delrieu o. Genomics. 1992 Dec;14(4):979-87. doi: 10.1016/s0888-7543(05)80120-x. Genomics. 1992. PMID: 1478676
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval.
Ducros A, Nagy T, Alamowitch S, Nibbio A, Joutel A, Vahedi K, Chabriat H, Iba-Zizen MT, Julien J, Davous P, Goas JY, Lyon-Caen O, Dubois B, Ducrocq X, Salsa F, Ragno M, Burkhard P, Bassetti C, Hutchinson M, Vérin M, Viader F, Chapon F, Levasseur M, Mas JL, Delrieu O, et al. Ducros A, et al. Among authors: delrieu o. Am J Hum Genet. 1996 Jan;58(1):171-81. Am J Hum Genet. 1996. PMID: 8554054 Free PMC article.
17 results