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Items: 1 to 20 of 211

1.

Genetic mapping in the Xp11.2 region of a new form of X-linked hypophosphatemic rickets.

Bolino A, Devoto M, Enia G, Zoccali C, Weissenbach J, Romeo G.

Eur J Hum Genet. 1993;1(4):269-79.

PMID:
7915957
2.

Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families.

Thakker RV, Davies KE, Read AP, Tippett P, Wooding C, Flint T, Wood S, Kruse TA, Whyte MP, O'Riordan JL.

Genomics. 1990 Oct;8(2):189-93.

PMID:
1979046
3.

Flanking markers define the X-linked hypophosphatemic rickets gene locus.

Econs MJ, Fain PR, Norman M, Speer MC, Pericak-Vance MA, Becker PA, Barker DF, Taylor A, Drezner MK.

J Bone Miner Res. 1993 Sep;8(9):1149-52.

PMID:
8237485
4.

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

Thakker RV, Read AP, Davies KE, Whyte MP, Weksberg R, Glorieux F, Davies M, Mountford RC, Harris R, King A, et al.

J Med Genet. 1987 Dec;24(12):756-60.

5.
6.

The human glycine receptor: a new probe that is linked to the X-linked hypophosphatemic rickets gene.

Econs MJ, Pericak-Vance MA, Betz H, Bartlett RJ, Speer MC, Drezner MK.

Genomics. 1990 Jul;7(3):439-41.

PMID:
2163973
7.

New insights into X-linked hypophosphatemia.

Grieff M.

Curr Opin Nephrol Hypertens. 1997 Jan;6(1):15-9. Review.

PMID:
9051349
8.
9.

Genetic linkage studies of X-linked hypophosphataemic rickets in a Saudi Arabian family.

Thakker RV, Farmery MR, Sakati NA, Milner RD.

Clin Endocrinol (Oxf). 1992 Oct;37(4):338-43.

PMID:
1483289
10.

The Gy mutation: another cause of X-linked hypophosphatemia in mouse.

Lyon MF, Scriver CR, Baker LR, Tenenhouse HS, Kronick J, Mandla S.

Proc Natl Acad Sci U S A. 1986 Jul;83(13):4899-903.

11.

Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets.

Eicher EM, Southard JL, Scriver CR, Glorieux FH.

Proc Natl Acad Sci U S A. 1976 Dec;73(12):4667-71.

12.

Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.

Scheinman SJ, Pook MA, Wooding C, Pang JT, Frymoyer PA, Thakker RV.

J Clin Invest. 1993 Jun;91(6):2351-7.

13.

Pex gene deletions in Gy and Hyp mice provide mouse models for X-linked hypophosphatemia.

Strom TM, Francis F, Lorenz B, Böddrich A, Econs MJ, Lehrach H, Meitinger T.

Hum Mol Genet. 1997 Feb;6(2):165-71.

PMID:
9063736
14.

Chromosomal localization of the human renal sodium phosphate transporter to chromosome 5: implications for X-linked hypophosphatemia.

Ghishan FK, Knobel S, Dasuki M, Butler M, Phillips J.

Pediatr Res. 1994 Apr;35(4 Pt 1):510-3.

PMID:
8047391
15.

Multilocus mapping of the X-linked hypophosphatemic rickets gene.

Econs MJ, Barker DF, Speer MC, Pericak-Vance MA, Fain PR, Drezner MK.

J Clin Endocrinol Metab. 1992 Jul;75(1):201-6.

PMID:
1352307
17.

A second family with XLRH displays the mutation S244L in the CLCN5 gene.

Oudet C, Martin-Coignard D, Pannetier S, Praud E, Champion G, Hanauer A.

Hum Genet. 1997 Jun;99(6):781-4.

PMID:
9187673
18.

X-linked hypophosphatemia.

Meyer RA Jr, Conway WF, Chan JC.

Semin Nephrol. 1989 Mar;9(1):56-61. Review.

PMID:
2662303
19.

Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis.

Read AP, Thakker RV, Davies KE, Mountford RC, Brenton DP, Davies M, Glorieux F, Harris R, Hendy GN, King A, et al.

Hum Genet. 1986 Jul;73(3):267-70.

PMID:
3015770
20.

Fine genetic mapping of the Hyp mutation on mouse chromosome X.

Du L, Desbarats M, Cornibert S, Malo D, Ecarot B.

Genomics. 1996 Mar 1;32(2):177-83.

PMID:
8833143

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