FISH CHARACTERIZATION OF THE XQ21 BREAKPOINT IN A TRANSLOCATION CARRIER WITH PREMATURE OVARIAN FAILURE

Authors
RIVA P MAGNANI I CONTI AMF GELLI D SALA C TONIOLO D LARIZZA L
Citation
P. Riva et al., FISH CHARACTERIZATION OF THE XQ21 BREAKPOINT IN A TRANSLOCATION CARRIER WITH PREMATURE OVARIAN FAILURE, Clinical genetics, 50(4), 1996, pp. 267-269
Citations number
9
Categorie Soggetti
Genetics & Heredity
Journal title
Clinical genetics → ACNP
ISSN journal
00099163
Volume
50
Issue
4
Year of publication
1996
Pages
267 - 269
Database
ISI
SICI code
0009-9163(1996)50:4<267:FCOTXB>2.0.ZU;2-U
Abstract
A panel of ordered YAC clones, isolated using STSs in the Xq13-Xq23 re gion, was used to characterize by Fluorescent In Situ Hybridization (F ISH) the Xq21 breakpoint in a t(X;1)(q21;p34) translocation female wit h premature ovarian failure. The YAC 949E11 was found to span the brea kpoint, but also to join the two non-overlapping YACs 36CB1 and 40AB3, proximal and distal, respectively, to the patient's Xq21 breakpoint.