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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. Hum Genet. 1982;62(4):327-32. doi: 10.1007/BF00304549. Hum Genet. 1982. PMID: 7166308
Deletion proximal to DXS68 locus (L1 probe site) in a boy with Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal hypoplasia.
Chelly J, Marlhens F, Dutrillaux B, Van Ommen GJ, Lambert M, Haioun B, Boissinot G, Fardeau M, Kaplan JC. Chelly J, et al. Hum Genet. 1988 Mar;78(3):222-7. doi: 10.1007/BF00291665. Hum Genet. 1988. PMID: 2894344
A t(X;15)(q23;q25) with Xq reactivation in a lymphoblastoid cell line from Fanconi anemia.
Kokalj-Vokac N, Saint-Ruf C, Lefrançois D, Viegas-Péquignot E, Lemieux N, Malfoy B, Dutrillaux B. Kokalj-Vokac N, et al. Cytogenet Cell Genet. 1991;57(1):11-5. doi: 10.1159/000133103. Cytogenet Cell Genet. 1991. PMID: 1855386
High recurrence of rearrangements involving chromosome 14 in an ataxia telangiectasia lymphoblastoid cell line and in its mutagen-treated derivatives.
Lefrançois D, Kokalj N, Viegas-Péquignot E, Montagnier L, Dutrillaux B. Lefrançois D, et al. Hum Genet. 1991 Mar;86(5):475-80. doi: 10.1007/BF00194636. Hum Genet. 1991. PMID: 1849869
High resolution R- and G-banding on the same preparation.
Dutrillaux B, Viegas-Pequignot E. Dutrillaux B, et al. Hum Genet. 1981;57(1):93-5. doi: 10.1007/BF00271176. Hum Genet. 1981. PMID: 7262875
Isoacentric and isocentric chromosomes originating after deletions of human chromosomes.
Dutrillaux B, Al Achkar W, Aledo R, Aurias A, Couturier J, Dutrillaux AM, Flüry-Herard A, Gerbault-Seureau M, Hoffschir F, Lamoliatte E, et al. Dutrillaux B, et al. Hum Genet. 1987 Jul;76(3):244-7. doi: 10.1007/BF00283616. Hum Genet. 1987. PMID: 3596598
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