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

Author:

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

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference16 articles.

1. Mendelian inheritance in man;McKusick, V.A.,1986

2. A genetic study of familial hypophosphataemia and vitamin D resistant rickets with a review of the literature;Winters, R.W.; Graham, J.B.; Williams, T.F.; McFalls, V.W.; Burnett, C.H.;Medicine,1958

3. Three additional kindreds of the sex linked dominant type with a genetic analysis for four such families;Burnett, C.H.; Dent, C.E.; Harper, C.; Warland, B.J.;Am J Hum Genet; Vitamin D resistant rickets. Analysis of twenty four pedigrees with hereditary and sporadic cases,1959

4. The rheumatic manifestations of metabolic bone disease;Davies, M.; Stanbury, S.W.;Clin Rheum Dis,1981

5. Mapping of human Xlinked hypophosphataemic rickets by multilocus linkage analysis;Read, A.P.; Thakker, R.V.; Davies, K.E.;Hum Genet,1986

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