LINKAGE OF NONSPECIFIC X-LINKED MENTAL-RETARDATION TO XQ21.31

被引:11
作者
JEDELE, KB
MICHELS, VV
SCHAID, DJ
SCHOWALTER, KV
THIBODEAU, SN
机构
[1] MAYO CLIN & MAYO FDN,MOLEC GENET LAB,ROCHESTER,MN 55905
[2] MAYO CLIN & MAYO FDN,DEPT MED GENET,ROCHESTER,MN 55905
[3] MAYO CLIN & MAYO FDN,DEPT STAT,ROCHESTER,MN 55905
[4] MAYO CLIN & MAYO FDN,DEPT LAB GENET,ROCHESTER,MN 55905
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1992年 / 43卷 / 1-2期
关键词
X-LINKED MENTAL RETARDATION; LINKAGE; DXYS1; MRX;
D O I
10.1002/ajmg.1320430166
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mental retardation unassociated with the Fragile X syndrome accounts for up to 60% of patients with X-linked mental retardation. In this investigation, we report on a family with mild non-specific X-linked mental retardation (MRX) without other apparent phenotypic abnormalities. Linkage analysis on 27 relatives using 18 polymorphic markers spanning the X-chromosome demonstrated close linkage to DXYS1 with a peak LOD score of 2.14 at a theta of 0. Numerous families with various types of MRX have now been studied by other investigators using molecular genetic techniques. In addition to the family described in this report, a number of these have demonstrated linkage to the DXYS1 locus. These data suggest that a gene for mental retardation may exist in the region of DXYS1. Alternatively, this area of the X-chromosome may harbor multiple different but closely linked genes which cause the various types of MRX.
引用
收藏
页码:436 / 442
页数:7
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