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The cell cycle of lymphocytes in Fanconi anemia.
Dutrillaux B, Aurias A, Dutrillaux AM, Buriot D, Prieur M. Dutrillaux B, et al. Among authors: prieur m. Hum Genet. 1982;62(4):327-32. doi: 10.1007/BF00304549. Hum Genet. 1982. PMID: 7166308
Inversion (14)(q12qter) or (q11.2q32.3): the most frequently acquired rearrangement in lymphocytes.
Aurias A, Couturier J, Dutrillaux AM, Dutrillaux B, Herpin F, Lamoliatte E, Lombard M, Muleris M, Paravatou M, Prieur M, et al. Aurias A, et al. Among authors: prieur m. Hum Genet. 1985;71(1):19-21. doi: 10.1007/BF00295660. Hum Genet. 1985. PMID: 4029952
DiGeorge syndrome and 22q11 rearrangements.
Augusseau S, Jouk S, Jalbert P, Prieur M. Augusseau S, et al. Among authors: prieur m. Hum Genet. 1986 Oct;74(2):206. doi: 10.1007/BF00282098. Hum Genet. 1986. PMID: 3770751 No abstract available.
Acquired chromosome rearrangements in human lymphocytes: effect of aging.
Prieur M, Al Achkar W, Aurias A, Couturier J, Dutrillaux AM, Dutrillaux B, Flüry-Herard A, Gerbault-Seureau M, Hoffschir F, Lamoliatte E, et al. Prieur M, et al. Hum Genet. 1988 Jun;79(2):147-50. doi: 10.1007/BF00280554. Hum Genet. 1988. PMID: 3164704
Increase of sister chromatid exchanges in excision repair deficient xeroderma pigmentosum.
Aledo R, Renault G, Prieur M, Avril MF, Chrétien B, Dutrillaux B, Aurias A. Aledo R, et al. Among authors: prieur m. Hum Genet. 1989 Feb;81(3):221-5. doi: 10.1007/BF00278992. Hum Genet. 1989. PMID: 2921029
Systematic analysis of 95 reciprocal translocations of autosomes.
Aurias A, Prieur M, Dutrillaux B, Lejeune J. Aurias A, et al. Among authors: prieur m. Hum Genet. 1978 Dec 29;45(3):259-82. doi: 10.1007/BF00278725. Hum Genet. 1978. PMID: 738728
Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations.
Luciani JJ, de Mas P, Depetris D, Mignon-Ravix C, Bottani A, Prieur M, Jonveaux P, Philippe A, Bourrouillou G, de Martinville B, Delobel B, Vallee L, Croquette MF, Mattei MG. Luciani JJ, et al. Among authors: prieur m. J Med Genet. 2003 Sep;40(9):690-6. doi: 10.1136/jmg.40.9.690. J Med Genet. 2003. PMID: 12960216 Free PMC article. No abstract available.
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders.
Jacquemont ML, Sanlaville D, Redon R, Raoul O, Cormier-Daire V, Lyonnet S, Amiel J, Le Merrer M, Heron D, de Blois MC, Prieur M, Vekemans M, Carter NP, Munnich A, Colleaux L, Philippe A. Jacquemont ML, et al. Among authors: prieur m. J Med Genet. 2006 Nov;43(11):843-9. doi: 10.1136/jmg.2006.043166. Epub 2006 Jul 13. J Med Genet. 2006. PMID: 16840569 Free PMC article.
NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome.
Borck G, Redon R, Sanlaville D, Rio M, Prieur M, Lyonnet S, Vekemans M, Carter NP, Munnich A, Colleaux L, Cormier-Daire V. Borck G, et al. Among authors: prieur m. J Med Genet. 2004 Dec;41(12):e128. doi: 10.1136/jmg.2004.026666. J Med Genet. 2004. PMID: 15591270 Free PMC article. No abstract available.
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