Le Mée F - Search Results

1

CD4(+), CD56(+) DC2 acute leukemia is characterized by recurrent clonal chromosomal changes affecting 6 major targets: a study of 21 cases by the Groupe Français de Cytogénétique Hématologique.

Leroux D, Mugneret F, Callanan M, Radford-Weiss I, Dastugue N, Feuillard J, Le Mée F, Plessis G, Talmant P, Gachard N, Uettwiller F, Pages MP, Mozziconacci MJ, Eclache V, Sibille C, Avet-Loiseau H, Lafage-Pochitaloff M. Leroux D, et al. Among authors: le mee f. Blood. 2002 Jun 1;99(11):4154-9. doi: 10.1182/blood.v99.11.4154. Blood. 2002. PMID: 12010820 Free article.

2

Expression of the multidrug resistance-associated P-glycoprotein (P-170) in 59 cases of de novo acute lymphoblastic leukemia: prognostic implications.

Goasguen JE, Dossot JM, Fardel O, Le Mee F, Le Gall E, Leblay R, LePrise PY, Chaperon J, Fauchet R. Goasguen JE, et al. Among authors: le mee f. Blood. 1993 May 1;81(9):2394-8. Blood. 1993. PMID: 8097634 Free article.

3

Jumping translocation in acute leukemia of myelomonocytic lineage: a case report and review of the literature.

Bernard M, Lemée F, Picard F, Ghandour C, Drenou B, Le Prise PY, Lamy T. Bernard M, et al. Leukemia. 2000 Jan;14(1):119-22. doi: 10.1038/sj.leu.2401637. Leukemia. 2000. PMID: 10637486 Review.

4

46,XX,t(15;21)/47,XX,15p-,+21 mosaicism in a child with Down's syndrome.

Lucas J, Le Mee F, Pluquailec K, Le Marec B, Journel H, Picard F. Lucas J, et al. Among authors: le mee f, le marec b. Ann Genet. 1986;29(2):104-6. Ann Genet. 1986. PMID: 2945509

5

[Trisomy 18 with prolonged survival. Case report of a girl followed to 6 years of age].

Roussey M, Le Marec B, Le Berre C, Le Mée F, Picard F, Sénécal J. Roussey M, et al. Among authors: le mee f, le marec b, le berre c. Pediatrie. 1979 Dec;34(8):819-26. Pediatrie. 1979. PMID: 545280 French. No abstract available.

6

[Pure trisomy 13q13-qter caused by aneusomic recombination of a maternal pericentric inversion].

Lucas J, Le Mée F, Picard F, Le Marec B, Junien C. Lucas J, et al. Among authors: le mee f, le marec b. Ann Genet. 1983;26(3):187-90. Ann Genet. 1983. PMID: 6606383 French.

7

[De novo interstitial deletion of the long arm of chromosome 2: 46,XXX,del(2)(q14q21), associated with premature craniosynostosis].

Lucas J, Faivre J, Le Mee F, Hubert S, Pluquailec K, Picard F. Lucas J, et al. Among authors: le mee f. Ann Genet. 1987;30(1):33-8. Ann Genet. 1987. PMID: 3498427 French.

8

[Trisomy 20p derived from a maternal pericentric inversion and brachymesophalangy of the index finger].

Lucas J, Le Mée F, Le Marec B, Pluquailec K, Journel H, Picard F. Lucas J, et al. Among authors: le mee f, le marec b. Ann Genet. 1985;28(3):167-71. Ann Genet. 1985. PMID: 3879151 French.

9

Turner's syndrome with X-isochromosome and Hashimoto's thyroiditis.

de Kerdanet M, Lucas J, Lemee F, Lecornu M. de Kerdanet M, et al. Clin Endocrinol (Oxf). 1994 Nov;41(5):673-6. doi: 10.1111/j.1365-2265.1994.tb01835.x. Clin Endocrinol (Oxf). 1994. PMID: 7828358

10

[Psychomotor instability: is it really a characteristic sign of trisomy 9P? (apropos of 3 cases)].

Le Marec B, Bouchard C, Boixel J, Le Berre C, Le Buanec MC, Le Mee F, Picard F, Senecal J. Le Marec B, et al. Among authors: le mee f, le buanec mc, le berre c. J Genet Hum. 1982 Oct;30(3):263-9. J Genet Hum. 1982. PMID: 7153771 French. No abstract available.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

25 results

Search Page

Filters