Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146.
We have constructed two YAC contigs in the Xp11.23-p11.22 interval of the human X chromosome, a region that was previously poorly characterized. One contig, of at least 1.4 Mb, links the pseudogene OATL1 to the genes GATA1, TFE3, and SYP and also contains loci implicated in Wiskott-Aldrich syndrome...
Glavni autori: | Fisher, S, Hatchwell, E, Chand, A, Ockenden, N, Monaco, A, Craig, I |
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Format: | Journal article |
Jezik: | English |
Izdano: |
1995
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Slični predmeti
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YAC CONTIGS AND PHYSICAL MAPPING OF XP11.23-]P11.22
od: Fisher, S, i dr.
Izdano: (1994) -
A 2-Mb YAC contig encompassing three loci (DXF34, DXS14, and DXS390) that lie between Xp11.2 translocation breakpoints associated with incontinentia pigmenti type 1.
od: Reed, V, i dr.
Izdano: (1994) -
Physical mapping in a YAC contig of 11 markers on the human X chromosome in Xp11.23.
od: Hagemann, T, i dr.
Izdano: (1994) -
Dinucleotide repeat polymorphisms from DXS106 and DXS227 YACs using a two stage approach.
od: Fairweather, N, i dr.
Izdano: (1993) -
Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22.
od: Pook, M, i dr.
Izdano: (1993)