An analysis of Xq deletions

We characterized by fluorescence in situ hybridization and Southern blotting 14 partial Xq monosomies, 11 due to terminal deletions and 3 secondary to X/autosome translocations. Three cases were mosaics with a XO cell line. In view of the possible role played by telomeres in chromosome segregation,...

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Veröffentlicht in:	Human genetics 1996-03, Vol.97 (3), p.375-381
Hauptverfasser:	MARASCHIO, P, TUPLER, R, BARBIERATO, L, DAINOTTI, E, LARIZZA, D, BERNARDI, F, HOELLER, H, GARAU, A, TIEPOLO, L
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Biological and medical sciences Blotting, Southern Chromosome aberrations Chromosome Mapping Female Gene Deletion Humans In Situ Hybridization, Fluorescence Karyotyping Medical genetics Medical sciences Middle Aged X Chromosome
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