DXS26 (HU16) IS LOCATED IN XQ21.1

被引：14

作者：

SANKILA, EM

BRUNS, GAP

SCHWARTZ, M

NIKOSKELAINEN, E

NIEBUHR, E

HODGSON, SV

WRIGHT, AF

DELACHAPELLE, A

机构：

[1] FOLKHALSAN INST GENET, SF-00290 HELSINKI, FINLAND

[2] HARVARD UNIV, SCH MED, DEPT PEDIAT, BOSTON, MA 02115 USA

[3] HARVARD UNIV, SCH MED, DEPT GENET, BOSTON, MA 02115 USA

[4] RIGSHOSP, DEPT PEDIAT, CLIN GENET SECT 4062, DK-2100 COPENHAGEN, DENMARK

[5] UNIV TURKU, DEPT OPHTHALMOL, SF-20520 TURKU 52, FINLAND

[6] UNIV COPENHAGEN, INST MED GENET, DK-2200 COPENHAGEN, DENMARK

[7] UNITED MED & DENT SCH GUYS & ST THOMASS HOSP, PEDIAT RES UNIT, LONDON SE1 9RT, ENGLAND

[8] WESTERN GEN HOSP, MRC, HUMAN GENET UNIT, EDINBURGH EH4 2XU, MIDLOTHIAN, SCOTLAND

来源：

HUMAN GENETICS | 1990年 / 85卷 / 01期

关键词：

D O I：

10.1007/BF00276335

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

We have localized a single-copy DNA probe, HU16 (locus DXS26), to Xq21.1. The probe was isolated from a human-mouse hybrid X;13 library and mapped with human-mouse hybrids containing different portions of the human X chromosome and DNA from male patients with different X-chromosomal deletions. The following order of loci is proposed: Xcen-(DXS72, DXS169)-(DXS232,DXS26)-DXS121-DXS233-DXS165 TCD-DXS95-DXYSl-Xqter. HU16 will be useful in the study of the putative genes that reside in Xq21 and whose defects lead to deafness and mental retardation. © 1990 Springer-Verlag.

引用

页码：117 / 120

页数：4

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