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Annales de Genetique

Articles from the last few issues of Annales de Genetique © Elsevier
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  • The history of cytogenetics Portraits of some pioneers
    Annales de Genetique, Vol. 46, No. 4. (October 2003), pp. 433-442.
    by S Gilgenkrantz, EM Rivera
  • FISH and PCR analyses in three patients with 45,X/46,X,idic(Y) karyotype: clinical and pathologic spectrum
    Annales de Genetique, Vol. 46, No. 4. (October 2003), pp. 443-448.
    by F Alvarez-Nava, M Soto, MC Martinez, M Prieto, Z Alvarez
  • Duane anomaly, congenital myopathy and severe scoliosis in sibs: new AR syndrome?
    Annales de Genetique, Vol. 46, No. 4. (October 2003), pp. 449-452.
    by A Verloes, JP Misson, P Gillet, C Baumann, M Spiritus, M Deprez
  • Familial interstitial deletion of chromosome 4 (p15.2p16.1)
    Annales de Genetique, Vol. 46, No. 4. (October 2003), pp. 453-458.
    by VS Tonk, SM Jalal, J Gonzalez, A Kennedy, GVN Velagaleti
  • Limb reduction defects in the first generation and deafness in the second generation of intrauterine exposed fetuses to diethylstilbestrol
    Annales de Genetique, Vol. 46, No. 4. (October 2003), pp. 459-465.
    by C Stoll, Y Alembik, B Dott
  • Gerstmann-Straussler-Scheinker disease with P102L-V129 mutation: a case with psychiatric manifestations at onset
    Annales de Genetique, Vol. 46, No. 4. (October 2003), pp. 467-469.
    by M Bianca, S Bianca, I Vecchio, R Raffaele, C Ingegnosi, F Nicoletti
  • De novo balanced translocation (2;10)(q24;q22) associated with mental retardation
    Annales de Genetique, Vol. 46, No. 4. (October 2003), pp. 471-473.
    by CB Santos, G Discepoli, F Pigliapoco, R Boy, MMG Pimentel
  • Paternal reciprocal translocation t(11;16)(p13;q24.3) in a Silver-Russel syndrome patient
    Annales de Genetique, Vol. 46, No. 4. (October 2003), pp. 475-478.
    by VB Rao, K Lily, K Seema, K Ghosh, M Dipika
  • Two 48,XXYY patients: clinical, cytogenetic and molecular aspects
    Annales de Genetique, Vol. 46, No. 4. (October 2003), pp. 479-481.
    by L Zelante, MR Piemontese, G Francioli, S Calvano
  • ”Cri-du-chat” syndrome in a patient born to a mother with a paracentric inversion of chromosome 5q
    Annales de Genetique, Vol. 46, No. 4. (October 2003), pp. 483-486.
    by S Bourthoumieu, F Esclaire, F Terro, MC Baclet, A Bedu, B Dufetelle, B Gilbert, D Barthe, C Yardin
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