THE LOCALIZATION OF A GENE CAUSING X-LINKED CLEFT-PALATE AND ANKYLOGLOSSIA (CPX) IN AN ICELANDIC KINDRED IS BETWEEN DXS326 AND DXYS1X

被引:23
作者
STANIER, P
FORBES, SA
ARNASON, A
BJORNSSON, A
SVEINBJORNSDOTTIR, E
WILLIAMSON, R
MOORE, G
机构
[1] UNIV ICELAND,NATL HOSP,DEPT PATHOL,IMMUNOGENET UNIT,REYKJAVIK,ICELAND
[2] UNIV ICELAND,NATL HOSP,DEPT PLAST SURG,REYKJAVIK,ICELAND
[3] UNIV ICELAND,NATL HOSP,DEPT PATHOL,CYTOGENET LAB,REYKJAVIK,ICELAND
[4] ST MARYS HOSP,SCH MED,DEPT BIOCHEM & MOLEC BIOL,LONDON W2 1PG,ENGLAND
关键词
D O I
10.1006/geno.1993.1370
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The locus responsible for X-linked, nonsyndromic cleft palate and/or ankyloglossia (CPX) has previously been mapped to the proximal long arm of the human X chromosome between Xq21.31 and q21.33 in an Icelandic kindred. We have extended these studies by analyzing an additional 14 informative markers in the family as well as including several newly investigated family members. Recombination analysis indicates that the CPX locus is more proximal than previously thought, within the interval Xq21.1-q21.31. Two recombinants place DXYS1X as the distal flanking marker, while one recombinant defines DXS326 as the proximal flanking marker, an interval of less than 5 cM. Each of the flanking markers recombines with the CPX locus, giving 2-point lod scores of Z(max) = 4.16 at θ = 0.08 (DXS326) and Z(max) = 5.80 at θ = 0.06 (DXYS1X). © 1993 Academic Press. All rights reserved.
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页码:549 / 555
页数:7
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