Chery M - Search Results

1

De novo methylation of tumour suppressor genes CDKN2A and CDKN2B is a rare finding in B-cell chronic lymphocytic leukaemia.

Martel V, Guerci A, Humbert JC, Gregoire MJ, Chery M, Lederlin P, Jonveaux P. Martel V, et al. Among authors: chery m. Br J Haematol. 1997 Nov;99(2):320-4. doi: 10.1046/j.1365-2141.1997.3953209.x. Br J Haematol. 1997. PMID: 9375748 Free article.

2

Characterisation of an inverted X chromosome (p11.2q21.3) associated with mental retardation using FISH.

Sloan-Béna F, Philippe C, LeHeup B, Wuilque F, Levy ER, Chéry M, Jonveaux P, Monaco AP. Sloan-Béna F, et al. Among authors: chery m. J Med Genet. 1998 Feb;35(2):146-50. doi: 10.1136/jmg.35.2.146. J Med Genet. 1998. PMID: 9507395 Free PMC article.

3

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

4

[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.

5

[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.

6

[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.

7

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

8

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

9

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

10

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

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