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Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia.
Guioli S, Arveiler B, Bardoni B, Notarangelo LD, Panina P, Duse M, Ugazio A, Oberlé I, de Saint Basile G, Mandel JL, et al. Guioli S, et al. Among authors: oberle i. Hum Genet. 1989 Dec;84(1):19-21. doi: 10.1007/BF00210664. Hum Genet. 1989. PMID: 2575070
Multilocus analysis of the fragile X syndrome.
Brown WT, Gross A, Chan C, Jenkins EC, Mandel JL, Oberlé I, Arveiler B, Novelli G, Thibodeau S, Hagerman R, et al. Brown WT, et al. Among authors: oberle i. Hum Genet. 1988 Mar;78(3):201-5. doi: 10.1007/BF00291662. Hum Genet. 1988. PMID: 3162224
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