Philippe C - Search Results

1

Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1.

van der Maarel SM, Scholten IH, Huber I, Philippe C, Suijkerbuijk RF, Gilgenkrantz S, Kere J, Cremers FP, Ropers HH. van der Maarel SM, et al. Among authors: philippe c. Hum Mol Genet. 1996 Jul;5(7):887-97. doi: 10.1093/hmg/5.7.887. Hum Mol Genet. 1996. PMID: 8817323

2

Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant gene.

Bonaventure J, Philippe C, Plessis G, Vigneron J, Lasselin C, Maroteaux P, Gilgenkrantz S. Bonaventure J, et al. Among authors: philippe c. Hum Genet. 1992 Sep-Oct;90(1-2):164-8. doi: 10.1007/BF00210766. Hum Genet. 1992. PMID: 1358786

3

Incontinentia pigmenti (type 1) and X;5 translocation.

Bitoun P, Philippe C, Cherif M, Mulcahy MT, Gilgenkrantz S. Bitoun P, et al. Among authors: philippe c. Ann Genet. 1992;35(1):51-4. Ann Genet. 1992. PMID: 1610121 Review.

4

A high-resolution interval map of the q21 region of the human X chromosome.

Philippe C, Arnould C, Sloan F, van Bokhoven H, van der Velde-Visser SD, Chery M, Ropers HH, Gilgenkrantz S, Monaco AP, Cremers FP. Philippe C, et al. Genomics. 1995 Jun 10;27(3):539-43. doi: 10.1006/geno.1995.1089. Genomics. 1995. PMID: 7558039 Free article.

5

Cloning and characterization of the human choroideremia gene.

van Bokhoven H, van den Hurk JA, Bogerd L, Philippe C, Gilgenkrantz S, de Jong P, Ropers HH, Cremers FP. van Bokhoven H, et al. Among authors: philippe c. Hum Mol Genet. 1994 Jul;3(7):1041-6. doi: 10.1093/hmg/3.7.1041. Hum Mol Genet. 1994. PMID: 7981670

6

Chromosome rearrangements and human gene mapping.

Gilgenkrantz S, Philippe C, Chery M. Gilgenkrantz S, et al. Among authors: philippe c. Biomed Pharmacother. 1994;48(5-6):225-30. doi: 10.1016/0753-3322(94)90137-6. Biomed Pharmacother. 1994. PMID: 7999983

7

Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpoint.

Chery M, Biancalana V, Philippe C, Malpuech G, Carla H, Gilgenkrantz S, Mandel JL, Hanauer A. Chery M, et al. Among authors: philippe c. Hum Genet. 1994 May;93(5):587-91. doi: 10.1007/BF00202829. Hum Genet. 1994. PMID: 8168840

8

The Noonan syndrome. The Nancy experience revisited.

Chery M, Philippe C, Worms AM, Gilgenkrantz S. Chery M, et al. Among authors: philippe c. Genet Couns. 1993;4(2):113-8. Genet Couns. 1993. PMID: 8357561

9

Physical mapping of DNA markers in the q13-q22 region of the human X chromosome.

Philippe C, Cremers FP, Chery M, Bach I, Abbadi N, Ropers HH, Gilgenkrantz S. Philippe C, et al. Genomics. 1993 Jul;17(1):147-52. doi: 10.1006/geno.1993.1296. Genomics. 1993. PMID: 8406446

10

Monosomy 21q: two cases of del(21q) and review of the literature.

Huret JL, Léonard C, Chery M, Philippe C, Schafei-Benaissa E, Lefaure G, Labrune B, Gilgenkrantz S. Huret JL, et al. Among authors: philippe c. Clin Genet. 1995 Sep;48(3):140-7. doi: 10.1111/j.1399-0004.1995.tb04074.x. Clin Genet. 1995. PMID: 8556821 Review.

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