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Annales De Genetique|January 1, 1985
Monosomy 20p due to a de novo del(20)(p12.2). Clinical and radiological delineation of the syndromeD García-Cruz, H Rivera, L O Barajas, et al.Annales De Genetique|January 1, 1985
46,X,i(Xq)/47,XX,+13 mosaicismM Igarashi, M Tsukahara, Y Sugio, et al.Annales De Genetique|January 1, 1985
Centric fission of chromosome 7 with 47,XX,del(7)(pter----cen::q21----qter)+cen fr karyotype in a mother and proximal 7q deletion in two malformed newbornsJ P Fryns, A Kleczkowska, C Limbos, et al.Annales De Genetique|January 1, 1985
[Familial transmission of deleted chromosome 22 [r(22)p0?] in two normal women]M Teyssier, N MoreauAnnales De Genetique|January 1, 1985
[Chromosomal phylogeny of 7 species of Sciurinae]D Petit, B DutrillauxAnnales De Genetique|January 1, 1985
[Chromosomes and carcinogenesis. Study on the evolution of an epithelial cell line of porcine origin]P Genest, A M BouillantAnnales De Genetique|January 1, 1985
[Analysis by reflection. A new method of observing human chromosomes]J LejeuneAnnales De Genetique|January 1, 1990
Risk of Down syndrome in relatives of trisomy 21 children. A case-control studyC Berr, E Borghi, M O Rethoré, et al.Annales De Genetique|January 1, 1990
Mitotic disturbances associated with inversion 9qh. A case reportS K Murthy, K PrabhakaraPageof 129