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Autor:
V S, Baranov, M V, Aseev, Z B, Rakisheva, N P, Kuleshov, G S, Marinicheva, A M, Bychkova, V D, Zukin, E A, Ledashcheva, D S, Amoashiĭ, T V, Kuznetsova
Publikováno v:
Genetika. 29(6)
63 families at-rist of Fragile X-syndrome (FraX) are subjected to Southern blot analysis with the DNA probes Ox1.9 and Ox0.55. Molecular studies have confirmed an initial clinical diagnosis of FraX in 26 families earlier studied cytogenetically and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d672ed799771370e8bc0c31a3f5935f
https://pubmed.ncbi.nlm.nih.gov/8370498
https://pubmed.ncbi.nlm.nih.gov/8370498
