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Annales De Genetique|January 1, 1987
[Polymorphism of p49 Y-specific probe in Papuas Baruyas of Papua New Guinea]S Breuil, L Hallé, J Ruffié, et al.
Annales De Genetique|January 1, 1985
Assignment to chromosome 12 of the gene coding for the human cell surface antigen CD9(p24) using the monoclonal antibody ALB6C Boucheix, Nguyen-van-Cong, J Y Perrot, et al.
Annales De Genetique|January 1, 1985
On atavisms and atavistic genesJ M Cantú, C Ruiz
Annales De Genetique|January 1, 1985
[Union of 2 carriers of a balanced translocation. Familial study of 3 generations]S Gilgenkrantz, M J Grégoire, M Chery, et al.
Annales De Genetique|January 1, 1985
Complex chromosomal rearrangement involving chromosomes 11, 13, 14 and 18 resulting in monosomy for 13q32----qterS A Al-Awadi, A S Teebi, T S Sundareshan
Annales De Genetique|January 1, 1985
[Recombination between the fragile site Xq27 and the gene for coagulation factor IX]A Landoulsi, M C de Blois, P Guérin, et al.
Annales De Genetique|January 1, 1985
Interstitial deletion 1p as a result of a de novo reciprocal 1p;2p translocationJ M Hertz, P H Jensen
Annales De Genetique|January 1, 1985
A male with two different familial autosomal fragile sites and a cytogenetically abnormal offspringA Smith, A Manuel, G Den Dulk, et al.
Annales De Genetique|September 1, 1978
[Del (13) (q33). Exclusion of esterase D (ESD) from 13q33 and q34]C Turleau, J Séger, J de Grouchy, et al.
Annales De Genetique|June 1, 1979
[Partial monosomy due to long-arm deletion of chromosome 11 : del (11) (q23) (author's transl)]C Léonard, C Courpotin, B Labrune, et al.
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