GENETIC-LINKAGE OF FAMILIAL EXPANSILE OSTEOLYSIS TO CHROMOSOME 18Q

被引:86
作者
HUGHES, AE
SHEARMAN, AM
WEBER, JL
BARR, RJ
WALLACE, RGH
OSTERBERG, PH
NEVIN, NC
MOLLAN, RAB
机构
[1] QUEENS UNIV BELFAST, DEPT ORTHOPAED SURG, BELFAST BT9 7AB, NORTH IRELAND
[2] MARSHFIELD MED RES FDN, MARSHFIELD, WI 54449 USA
关键词
D O I
10.1093/hmg/3.2.359
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Familial expansile osteolysis is a rare bone dysplasia which is transmitted as an autosomal dominant trait in a large kindred in Northern Ireland. The gene which causes the disease shows tight linkage with several polymorphic markers on chromosome 18q with a maximum lod score of 11.53 at a recombination fraction of 0.00 with D18S64. The gene is flanked by D18S35 and D18S61 and is located at chromosome 18q21.1 - q22. Mapping a new locus for a gene involved in regulation of bone metabolism may also have implications in the study of Paget's disease of bone which is a common related bone dysplasia.
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收藏
页码:359 / 361
页数:3
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