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Annales De Genetique|January 1, 1996
Centromeric alphoid sequences are breakage prone resulting in pericentromeric inversion heteromorphism of qh region of chromosome 1R S Verma, K H Ramesh, T Mathews, et al.Annales De Genetique|January 1, 1996
Down syndrome with unusual chromosome translocation: case report and reviewL Bruni, R Capolino, M C Tozzi, et al.Annales De Genetique|January 1, 1996
Mapping of 22 YACs on human chromosomes by fish using yeast DNA Alu-PCR products for competitionA F Goguel, F Pulcini, G Danglot, et al.Annales De Genetique|January 1, 1996
Autosomal folate sensitive fragile sites in an autistic Basque sampleI Arrieta, T Nuñez, A Gil, et al.Annales De Genetique|January 1, 1996
Interstitial deletion 6q16.2q22.2 in a child with ectrodactylyL Correa-Cerro, D Garcíaz-Cruz, L Díaz-Castaños, et al.Annales De Genetique|January 1, 1996
Synaptic behaviour of sex chromosome in two XYY menO Gabriel-Robez, B Delobel, M F Croquette, et al.Annales De Genetique|January 1, 1996
Identification of a cat eye syndrome using DNA sequence dosage analysisF Bulle, J Lespinasse, A Pawlak, et al.Annales De Genetique|January 1, 1996
Translocation t(10;11) involving the MLL gene in acute myeloid leukemia. Importance of fluorescence in situ hybridization (FISH) analysisR Berger, M Le Coniat, M A Flexor, et al.Annales De Genetique|January 1, 1996
Further delineation of 7p trisomy. Case report and review of literatureR Pallotta, L Dalprà, P Fusilli, et al.Annales De Genetique|January 1, 1993
[Importance of mutations interfering with mouse development]J L GuenetPageof 129