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Annales De Genetique|February 16, 2000
Novel translocation t(3;11)(p21;q24) in multiple myeloma characterised by FISHA Smith, R de Lambert, L RobsonAnnales De Genetique|February 16, 2000
Schinzel-Giedion syndrome with severe deafness and neurodegenerative processY Alembik, D Christmann, A de Saint Martin, et al.Annales De Genetique|December 1, 1975
[Pericentric inversion of no. 3, homozygous and heterozygous, and centromeric transposition of no. 12 in a family of orangutans. Implications for evolution]C Turleau, J de Grouchy, C Chavin-ColinAnnales De Genetique|December 1, 1975
Identification of isochromosome 17 in a girl with mental retardation and congenital malformationsF Salamanca-Gómez, S ArmendaresAnnales De Genetique|December 1, 1975
Chromosome band analysis in 19 cases of chronic myeloid leukemia: 9 chronic, 10 blastic, two with Ph1 (22q-) translocation on 17 short armE Engel, B J McGee, J M Flexner, et al.Annales De Genetique|December 1, 1975
[A second example of telomeric fusion 2 X chromosomes]J Fraisse, C Laurent, N Collard, et al.Annales De Genetique|December 1, 1975
[Partial 11q monosomy and trigonocephaly. A new syndrome]C Turleau, F Chavin-Colin, M Roubin, et al.Annales De Genetique|June 1, 1976
[Partial trisomy of the long arm of the chromosme 11 by malsegregation of a maternal translocation t(11;22)(q23 1;q1 11)]B Noel, M Levy, M O RethoréAnnales De Genetique|September 1, 1975
Milk casein polymorphism in the Kikuyu populationA Ponzone, G F Voglino, A TognoloAnnales De Genetique|September 1, 1976
[Chromosome effect of cyclophosphamide in various strains of mice]I Emerit, A Levy, J FeingoldPageof 129