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Annales De Genetique|March 31, 2004
Double trisomy (48,XXY,+21) in monozygotic twins: case report and review of the literatureDimitrios Iliopoulos, George Poultsides, Vasiliki Peristeri, et al.Annales De Genetique|January 1, 1992
Cystic fibrosis gene mutations and linked RFLPs in the Slovenian populationM Ravnik-Glavac, P Gasparini, B Peterlin, et al.Annales De Genetique|January 1, 1992
Mapping of the Darier's disease gene by serogenetic markers: results in two large British kindredsC S Munro, S S Mastana, S S PapihaAnnales De Genetique|April 2, 2003
Tetraploid/diploid mosaicism: case report and review of the literatureLuís Alonso, Isabel Melaragno, Adriana Bortolai, et al.Annales De Genetique|June 24, 2003
Study of placenta of children born with congenital malformationsClaude Stoll, Yves Alembik, Béatrice Dott, et al.Annales De Genetique|June 24, 2003
Holt-Oram syndrome: a new mutation in the TBX5 gene in two unrelated familiesClaudia Gruenauer-Kloevekorn, Ursula G FrosterAnnales De Genetique|June 24, 2003
Pure partial trisomy 6p due to a familial insertion (16;6)(p12;p21.2p23)María G Domínguez, Luis E Wong-Ley, Horacio Rivera, et al.Annales De Genetique|January 1, 1992
Ring chromosome 17. Case report and review of the literatureM Teyssier, C Charrin, G Corgiolu Theuil, et al.Annales De Genetique|December 9, 2003
Duane anomaly, congenital myopathy and severe scoliosis in sibs: new AR syndrome?Alain Verloes, Jean-Paul Misson, Philippe Gillet, et al.Annales De Genetique|December 9, 2003
Limb reduction defects in the first generation and deafness in the second generation of intrauterine exposed fetuses to diethylstilbestrolC Stoll, Y Alembik, B DottPageof 129