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

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 f...

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Bibliografske podrobnosti
Main Authors: Thakker, R V, Read, A P, Davies, K E, Whyte, M P, Weksberg, R, Glorieux, F, Davies, M, Mountford, R C, Harris, R, King, A
Format: Artigo
Jezik:Inglês
Izdano: 1987
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050404/
https://ncbi.nlm.nih.gov/pubmed/2828625
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