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Applications de l'hybridation in situ fluorescente (FISH) dans le diagnostic prénatal

  • Seminar Über Neues Aus Der Gynäkologie Und Geburtshilfe
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Archives of Gynecology and Obstetrics Aims and scope Submit manuscript

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Références

  1. Lichter P et al. (1988) Rapid detection of human chromosome 21 aberrations by in situ hybridization. Proc Natl Acad Sci USA 85:9664–9668

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  2. Thonney F, Pescia G (1993) Hybridation fluorescente in situ (FISH) et cytogénétique moléculaire. Rev Med Suisse Rom 113:305–308

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  3. Ward BE et al. (1993) Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4500 specimens. Am J Hum Genet 52:854–865

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Authors and Affiliations

  1. Division autonome de Génétique médicale, CHUV, CH-1011, Lausanne, Switzerland

    G. Pescia, S. Fokstuen & F. Thonney

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  1. G. Pescia
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  2. S. Fokstuen
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  3. F. Thonney
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Pescia, G., Fokstuen, S. & Thonney, F. Applications de l'hybridation in situ fluorescente (FISH) dans le diagnostic prénatal. Arch Gynecol Obstet 255 (Suppl 2), S367–S371 (1994). https://doi.org/10.1007/BF02389259

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  • DOI: https://doi.org/10.1007/BF02389259

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