Chéry M - Search Results

1

X chromosome inactivation in 30 girls with Rett syndrome: analysis using the probe.

Camus P, Abbadi N, Perrier MC, Chéry M, Gilgenkrantz S. Camus P, et al. Among authors: chery m. Hum Genet. 1996 Feb;97(2):247-50. doi: 10.1007/BF02265275. Hum Genet. 1996. PMID: 8566963

2

Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb region.

Dahl N, Hu LJ, Chery M, Fardeau M, Gilgenkrantz S, Nivelon-Chevallier A, Sidaner-Noisette I, Mugneret F, Gouyon JB, Gal A, et al. Dahl N, et al. Among authors: chery m. Am J Hum Genet. 1995 May;56(5):1108-15. Am J Hum Genet. 1995. PMID: 7726166 Free PMC article.

3

Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivation.

Abbadi N, Philippe C, Chery M, Gilgenkrantz H, Tome F, Collin H, Theau D, Recan D, Broux O, Fardeau M, et al. Abbadi N, et al. Among authors: chery m. Am J Med Genet. 1994 Aug 15;52(2):198-206. doi: 10.1002/ajmg.1320520215. Am J Med Genet. 1994. PMID: 7802009

4

Chromosome rearrangements and human gene mapping.

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

5

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. Hum Genet. 1994 May;93(5):587-91. doi: 10.1007/BF00202829. Hum Genet. 1994. PMID: 8168840

6

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. Among authors: chery m. Genomics. 1993 Jul;17(1):147-52. doi: 10.1006/geno.1993.1296. Genomics. 1993. PMID: 8406446

7

Distal trisomy 14q. I. Clinical and cytogenetical studies.

Gilgenkrantz S, Vigneron J, Peter MO, Dufier JL, Teboul M, Chery M, Keyeux G, Lefranc MP. Gilgenkrantz S, et al. Among authors: chery m. Hum Genet. 1990 Oct;85(6):612-6. doi: 10.1007/BF00193584. Hum Genet. 1990. PMID: 2227953 Review.

8

A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1.

Abbas N, Novelli G, Stella NC, Triolo O, Corrado F, Fellous M, Chery M, Gilgenkrantz S, Dallapiccola B. Abbas N, et al. Among authors: chery m. Hum Genet. 1990 Nov;86(1):94-8. doi: 10.1007/BF00205184. Hum Genet. 1990. PMID: 2253943

9

The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15.

Hanauer A, Chery M, Fujita R, Driesel AJ, Gilgenkrantz S, Mandel JL. Hanauer A, et al. Among authors: chery m. Am J Hum Genet. 1990 Jan;46(1):133-7. Am J Hum Genet. 1990. PMID: 2294745 Free PMC article.

10

The Noonan syndrome. The Nancy experience revisited.

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

58 results

Search Page