Search Results - Tihy, F

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  1. 1
    Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype

    Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype by D'Amours, G, Kibar, Z, Mathonnet, G, Fetni, R, Tihy, F, Désilets, V, Nizard, S, Michaud, JL, Lemyre, E

    Published in Clinical genetics
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  2. 2
    Randomised trial to assess safety and fetal outcome of early and midtrimester amniocentesis

    Randomised trial to assess safety and fetal outcome of early and midtrimester amniocentesis by Wilson, R, Johnson, J, Dansereau, J

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  3. 3
    Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay

    Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay by Uddin, Mohammed, Pellecchia, Giovanna, Thiruvahindrapuram, Bhooma, D’Abate, Lia, Merico, Daniele, Chan, Ada, Zarrei, Mehdi, Tammimies, Kristiina, Walker, Susan, Gazzellone, Matthew J., Nalpathamkalam, Thomas, Yuen, Ryan K. C., Devriendt, Koenraad, Mathonnet, Géraldine, Lemyre, Emmanuelle, Nizard, Sonia, Shago, Mary, Joseph-George, Ann M., Noor, Abdul, Carter, Melissa T., Yoon, Grace, Kannu, Peter, Tihy, Frédérique, Thorland, Erik C., Marshall, Christian R., Buchanan, Janet A., Speevak, Marsha, Stavropoulos, Dimitri J., Scherer, Stephen W.

    Published in Scientific reports
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  4. 4
    Complex chromosome rearrangement and recombinant balanced translocation in a mother and a daughter with the same phenotypic abnormalities

    Complex chromosome rearrangement and recombinant balanced translocation in a mother and a daughter with the same phenotypic abnormalities by Tihy, Frédérique, Lemieux, N., Lemyre, E.

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  5. 5
    Cytogenetic Analysis of a Parachordoma

    Cytogenetic Analysis of a Parachordoma by Tihy, Frédérique, Scott, Patrick, Russo, Pierre, Champagne, Martin, Tabet, Jean-Claude, Lemieux, Nicole

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  6. 6
    Activation of the catalytic core of a group I intron by a remote 3' splice junction

    Activation of the catalytic core of a group I intron by a remote 3' splice junction by MICHEL, F, JAEGER, L, WESTHOF, E, KURAS, R, TIHY, F, MING-QUN XU, SHUB, D. A

    Published in Genes & development
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  7. 7
    Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughter

    Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughter by TIHY, F, VOGT, N, DUTRILLAUX, B, LEMIEUX, N, RECAN, D, MALFOY, B, LETURCQ, F, COQUET, M, SERVILLE, F, FONTAN, D, GUILLARD, J.-M, KAPLAN, J.-C

    Published in Human genetics
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  8. 8
    Frequencies of chromosomal abnormalities at amniocentesis: Over 20 years of cytogenetic analyses in one laboratory

    Frequencies of chromosomal abnormalities at amniocentesis: Over 20 years of cytogenetic analyses in one laboratory by Caron, Lorraine, Tihy, Frédérique, Dallaire, Louis

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  9. 9
    Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p

    Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p by Tihy, Frédérique, Lemyre, Emmanuelle, Dallaire, Louis, Lemieux, Nicole

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  10. 10
    De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype

    De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype by Tihy, Frédérique, Lemyre, Emmanuelle, Lemieux, Nicole, Dallaire, Louis

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  11. 11
    PTPRD copy number variants and Ewing's sarcoma: Strengthening the association and therapeutic implications

    PTPRD copy number variants and Ewing's sarcoma: Strengthening the association and therapeutic implications by Saskin, Avi, Seath, Kimberly, Tihy, Frederique, Lemyre, Emmanuelle, Davis, Jeffrey, Halal, Fahed, Armstrong, Linlea

    Published in Cancer genetics
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