Glorieux FH - Search Results

1

Linkage mapping by simultaneous screening of multiple polymorphic loci using Alu oligonucleotide-directed PCR.

Zietkiewicz E, Labuda M, Sinnett D, Glorieux FH, Labuda D. Zietkiewicz E, et al. Among authors: glorieux fh. Proc Natl Acad Sci U S A. 1992 Sep 15;89(18):8448-51. doi: 10.1073/pnas.89.18.8448. Proc Natl Acad Sci U S A. 1992. PMID: 1528850 Free PMC article.

2

Two hereditary defects related to vitamin D metabolism map to the same region of human chromosome 12q13-14.

Labuda M, Fujiwara TM, Ross MV, Morgan K, Garcia-Heras J, Ledbetter DH, Hughes MR, Glorieux FH. Labuda M, et al. Among authors: glorieux fh. J Bone Miner Res. 1992 Dec;7(12):1447-53. doi: 10.1002/jbmr.5650071212. J Bone Miner Res. 1992. PMID: 1336301

3

Mapping autosomal recessive vitamin D dependency type I to chromosome 12q14 by linkage analysis.

Labuda M, Morgan K, Glorieux FH. Labuda M, et al. Among authors: glorieux fh. Am J Hum Genet. 1990 Jul;47(1):28-36. Am J Hum Genet. 1990. PMID: 1971995 Free PMC article.

4

Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians.

Labuda M, Labuda D, Korab-Laskowska M, Cole DE, Zietkiewicz E, Weissenbach J, Popowska E, Pronicka E, Root AW, Glorieux FH. Labuda M, et al. Among authors: glorieux fh. Am J Hum Genet. 1996 Sep;59(3):633-43. Am J Hum Genet. 1996. PMID: 8751865 Free PMC article.

5

Human 25-hydroxyvitamin D 24-hydroxylase cytochrome P450 subunit maps to a different chromosomal location than that of pseudovitamin D-deficient rickets.

Labuda M, Lemieux N, Tihy F, Prinster C, Glorieux FH. Labuda M, et al. Among authors: glorieux fh. J Bone Miner Res. 1993 Nov;8(11):1397-406. doi: 10.1002/jbmr.5650081114. J Bone Miner Res. 1993. PMID: 8266831

6

Osteogenesis imperfecta type VII maps to the short arm of chromosome 3.

Labuda M, Morissette J, Ward LM, Rauch F, Lalic L, Roughley PJ, Glorieux FH. Labuda M, et al. Among authors: glorieux fh. Bone. 2002 Jul;31(1):19-25. doi: 10.1016/s8756-3282(02)00808-6. Bone. 2002. PMID: 12110407

7

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. Read AP, et al. Hum Genet. 1986 Jul;73(3):267-70. doi: 10.1007/BF00401242. Hum Genet. 1986. PMID: 3015770

8

Phosphate transport by osteoblasts from X-linked hypophosphatemic mice.

Ecarot B, Caverzasio J, Desbarats M, Bonjour JP, Glorieux FH. Ecarot B, et al. Among authors: glorieux fh. Am J Physiol. 1994 Jan;266(1 Pt 1):E33-8. doi: 10.1152/ajpendo.1994.266.1.E33. Am J Physiol. 1994. PMID: 8304442

9

Polymerase chain reaction-based technique for the selective enrichment and analysis of mosaic arg201 mutations in G alpha s from patients with fibrous dysplasia of bone.

Candeliere GA, Roughley PJ, Glorieux FH. Candeliere GA, et al. Among authors: glorieux fh. Bone. 1997 Aug;21(2):201-6. doi: 10.1016/s8756-3282(97)00107-5. Bone. 1997. PMID: 9267696

10

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. Thakker RV, et al. J Med Genet. 1987 Dec;24(12):756-60. doi: 10.1136/jmg.24.12.756. J Med Genet. 1987. PMID: 2828625 Free PMC article.

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