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Three DNA markers for hypophosphataemic rickets.
Rowe PS, Read AP, Mountford R, Benham F, Kruse TA, Camerino G, Davies KE, O'Riordan JL. Rowe PS, et al. Hum Genet. 1992 Jul;89(5):539-42. doi: 10.1007/BF00219180. Hum Genet. 1992. PMID: 1353055
Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP).
Rowe PS, Oudet CL, Francis F, Sinding C, Pannetier S, Econs MJ, Strom TM, Meitinger T, Garabedian M, David A, Macher MA, Questiaux E, Popowska E, Pronicka E, Read AP, Mokrzycki A, Glorieux FH, Drezner MK, Hanauer A, Lehrach H, Goulding JN, O'Riordan JL. Rowe PS, et al. Among authors: o riordan jl. Hum Mol Genet. 1997 Apr;6(4):539-49. doi: 10.1093/hmg/6.4.539. Hum Mol Genet. 1997. PMID: 9097956
Gene mapping of mineral metabolic disorders.
Thakker RV, Davies KE, O'Riordan JL. Thakker RV, et al. J Inherit Metab Dis. 1989;12 Suppl 1:231-46. doi: 10.1007/BF01799298. J Inherit Metab Dis. 1989. PMID: 2681997 Review.
Dinucleotide repeat polymorphism at the DXS1683 locus.
Econs MJ, Francis F, Rowe PS, Speer MC, O'Riordan JL, Lehrach H, Becker PA. Econs MJ, et al. Hum Mol Genet. 1994 Apr;3(4):680. doi: 10.1093/hmg/3.4.680. Hum Mol Genet. 1994. PMID: 8069326 No abstract available.
180 results