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Annales De Genetique|March 1, 1978
A 45,XX,-5,-14,+t(5q;14q)mat cri du chat childH N Bass, R S Sparkes, B F Crandall, et al.
Annales De Genetique|January 1, 1985
Monozygotic twins with Turner's syndrome and mos 45,X/46,X,r,(Y)J C de Almeida, J C Llerena, R Rita Martins, et al.
Annales De Genetique|January 1, 1985
Deletion of the proximal long arm of chromosome 3 in an infant with features of Turner syndromeM B Jenkins, H J Stang, E Davis, et al.
Annales De Genetique|January 1, 1985
De novo partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosisJ P Fryns, M Haspeslagh, A Agneessens, et al.
Annales De Genetique|January 1, 1985
Unusual chromosome 9 polymorphism and reproductive failureJ P Fryns, A Kleczkowska, L Londers, et al.
Annales De Genetique|January 1, 1985
Partial trisomy 11p with interatrial septal aneurysm. Case report and literature reviewK Aleck, J Williams, C Mongkolsmai, et al.
Annales De Genetique|January 1, 1985
19q distal trisomy due to a de novo (19;22)(q13.2;p11) translocationF Rivas, D García-Cruz, H Rivera, et al.
Annales De Genetique|January 1, 1985
A case of male pseudohermaphroditism with normal androgen receptor binding and 47,XYY karyotypeJ M Bosch-Banyeras, L Audi, E Sarret, et al.
Annales De Genetique|January 1, 1985
Trisomy 11p15 and Beckwith-Wiedemann syndrome. Report of two new casesH Journel, J Lucas, C Allaire, et al.
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