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Annales De Genetique|December 8, 2004
A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES)J Lespinasse, H Testard, F Nugues, et al.Annales De Genetique|December 8, 2004
Prevalence of C282Y and H63D mutations in the haemochromatosis (HFE) gene in Tunisian populationR Sassi, Slama Hmida, H Kaabi, et al.Annales De Genetique|September 1, 2004
Auricular mild errors of morphogenesis: epidemiological analysis, local correlations and clinical significanceDavid Bader, Marta Grun, Shlomit Riskin-Mashiah, et al.Annales De Genetique|September 1, 2004
Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15)Monica C Varela, Graziela M P Lopes, Celia P KoiffmannAnnales De Genetique|September 1, 2004
Inherited ring chromosome 8 without loss of subtelomeric sequencesCedric Le Caignec, Michelle Boceno, Sebastien Jacquemont, et al.Annales De Genetique|December 2, 1998
Duplication 10q22.1-q25.1 due to intrachromosomal insertion: a second caseP W Goss, L Voullaire, R J GardnerAnnales De Genetique|January 1, 1997
Cytogenetic characterization of interspecific somatic hybrids by PRINSP Coullin, B Andreo, J J Candelier, et al.Annales De Genetique|January 1, 1997
Prevalence, male germ-line origin and new patterns of inversions in haemophilia AS Valleix, K Nafa, N Stieltjes, et al.Annales De Genetique|January 1, 1997
Collaborative study of mosaic tetrasomy 12p or Pallister-Killian syndrome (nineteen fetuses or children)M Mathieu, C Piussan, F Thepot, et al.Annales De Genetique|January 1, 1997
Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic featuresA Mégarbané, N Souraty, D Theophile, et al.Pageof 129