Chery M - Search Results

1

[Fragile site on chromosome 2 (q11) in a case of familial lymphohistiocytosis].

Gilgenkrantz S, Gregoire MJ, Chery M, Bordigoni P, Olive D. Gilgenkrantz S, et al. Among authors: chery m. J Genet Hum. 1984 Jul;32(3):209-19. J Genet Hum. 1984. PMID: 6434696 French.

2

[Balanced X-autosomal translocation and mental retardation. Mapping mental retardation linked to X (excluding fragile X)].

Teboul M, Mujica P, Chery M, Leotard B, Gilgenkrantz S. Teboul M, et al. Among authors: chery m. J Genet Hum. 1989 Sep;37(3):179-95. J Genet Hum. 1989. PMID: 2625622 French.

3

[Union of 2 carriers of a balanced translocation. Familial study of 3 generations].

Gilgenkrantz S, Grégoire MJ, Chery M, Defèche C. Gilgenkrantz S, et al. Among authors: chery m. Ann Genet. 1985;28(3):164-6. Ann Genet. 1985. PMID: 3879150 French.

4

Sublocalisation of the X breakpoint in the translocation (X; 18)(p11.2; q11.2) primary change in synovial sarcomas.

Gilgenkrantz S, Chery M, Teboul M, Mujica P, Leotard B, Gregoire MJ, Boman F, Duprez A, Hanauer A. Gilgenkrantz S, et al. Among authors: chery m. Oncogene. 1990 Jul;5(7):1063-6. Oncogene. 1990. PMID: 2165233

5

Interstitial deletion of the long arm of chromosome 6.

Chery M, Formiga LF, Mujica P, André M, Stehelin D, Dozier C, Gilgenkrantz S. Chery M, et al. Ann Genet. 1989;32(2):82-6. Ann Genet. 1989. PMID: 2757364

6

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

7

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.

8

[Familial supravalvular aortic stenosis. Investigation in a family and review of the literature].

Burnel P, Marçon F, Lucron H, Bosser G, Gilgenkrantz S, Jonveaux P, Chéry M, Worms AM. Burnel P, et al. Among authors: chery m. Arch Mal Coeur Vaiss. 1997 May;90(5):719-24. Arch Mal Coeur Vaiss. 1997. PMID: 9295957 Review. French.

9

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

10

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.

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