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Journal article

Bridging markers defining the map position of X linked hypophosphataemic rickets.

Abstract:

Hypophosphataemic rickets is commonly an X linked dominant hereditary disorder associated with a renal tubular defect in phosphate transport and bone deformities. The gene causing this disorder has been mapped to Xp22.31----p21.3 by using cloned human X chromosome sequences identifying restriction fragment length polymorphisms (RFLPs) in linkage studies of affected families. The hypophosphataemic rickets gene locus (HPDR) was previously mapped distal to the X linked polymorphic locus DXS41 (9...

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Publication status:
Published

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Publisher copy:
10.1136/jmg.24.12.756

Authors


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Institution:
University of Oxford
Department:
Oxford, MSD, RDM, OCDEM
Davies, KE More by this author
Weksberg, R More by this author
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Journal:
Journal of medical genetics
Volume:
24
Issue:
12
Pages:
756-760
Publication date:
1987-12-05
DOI:
EISSN:
1468-6244
ISSN:
0022-2593
URN:
uuid:e04846f3-dce0-4624-b5f0-10b6b4293652
Source identifiers:
24658
Local pid:
pubs:24658

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