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Annales De Genetique|January 1, 1994
The meiotic pairing behaviour in human spermatocytes carrier of chromosome anomalies and their repercussions on reproductive fitness. I: Inversions and insertions. A European collaborative studyO Gabriel-Robez, Y RumplerAnnales De Genetique|January 1, 1979
Clinical significance of the satellited short arm of human chromosome 17 (17ps +) : a rare heteromorphism?R S Verma, S Ved Brat, J Warman, et al.Annales De Genetique|January 1, 1979
Supernumerary chromosome possibly representing segment p11 yields q14 of chromosome 2H S Wang, A G HunterAnnales De Genetique|January 1, 1979
Type and contretype signs in monosomy and trisomy 9p. On a case 46,XY, del (9) (pter yields p12:)A Hernandez, H Rivera, M Jiménez-Sainz, et al.Annales De Genetique|January 1, 1979
[Distal 9q trisomy phenotype in a patient with a supernumerary rearranged chromosome [t(X:9)] (author's transl)]G Pescia, M Jotterand-Bellomo, H de Crousaz, et al.Annales De Genetique|January 1, 1989
Inherited pericentric inversion of Y-chromosome with trisomy 21. A case reportD S Krishna Murthy, S K Murthy, J K Patel, et al.Annales De Genetique|January 1, 1986
[Strategies for detecting restriction polymorphisms of Y chromosome sequences]K Y Ngo, G LucotteAnnales De Genetique|January 1, 1989
Duplication 7p de novo and literature reviewK Zerres, G Schwanitz, K Gellissen, et al.Annales De Genetique|January 1, 1989
The decrease of catalase or esterase D activity in patients with microdeletions of 11p or 13q does not increase their radiosensitivityL Sabatier, F Hoffschir, W A al Achkar, et al.Pageof 129