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Annales De Genetique|January 1, 1979
Trisomy 3q : two clinically similar but cytogenetically different casesM T Mulcahy, P J Pemberton, P SpragueAnnales De Genetique|January 1, 1979
Some clinical and cytogenetic observations on a ring chromosome 13 (p11 q34)A Hernandez, D Garcia-Cruz, L Plascencia, et al.Annales De Genetique|January 1, 1987
A case of interstitial 1q deletion [46,XY,del(q25q32.1)]S Hamano, Y Fukushima, T Yamada, et al.Annales De Genetique|January 1, 1987
[Partial deletion 10qter. A new case]P Vanlieferinghen, P Dechelotte, F CharbonnéAnnales De Genetique|January 1, 1987
The beta amyloid protein (AD-AP) cDNA hybridizes in normal and Alzheimer individuals near the interface of 21q21 and q22.1V Blanquet, D Goldgaber, C Turleau, et al.Annales De Genetique|January 1, 1987
Partial monosomy 22 as result of an X/22 translocation in a newborn with DiGeorge syndromeG Schwanitz, K ZerresAnnales De Genetique|January 1, 1987
[A rare polydysmorphic syndrome: leprechaunism. Review of 49 cases reported in the literature]A Cantani, M G Ziruolo, M L TacconiAnnales De Genetique|January 1, 1988
Trisomy 8p by malsegregation of a t(5;8)(p15;p11)mat in a case of XY pure gonadal dysgenesisL Memo, E Lenzini, C BaccichettiAnnales De Genetique|December 1, 1977
[A theoretical model of structural chromosome rearrangement induction]B DutrillauxAnnales De Genetique|January 1, 1987
[De novo interstitial deletion of the long arm of chromosome 2: 46,XXX,del(2)(q14q21), associated with premature craniosynostosis]J Lucas, J Faivre, F Le Mee, et al.Pageof 129