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Page 1
Validation of image processing tools for 3-D fluorescence microscopy.
Dieterlen A, Xu C, Gramain MP, Haeberlé O, Colicchio B, Cudel C, Jacquey S, Ginglinger E, Jung G, Jeandidier E. Dieterlen A, et al. Among authors: jeandidier e. C R Biol. 2002 Apr;325(4):327-34. doi: 10.1016/s1631-0691(02)01448-8. C R Biol. 2002. PMID: 12161912 Free article.
Intrachromosomal triplication for the distal part of chromosome 15q.
Schluth C, Mattei MG, Mignon-Ravix C, Salman S, Alembik Y, Willig J, Ginglinger E, Jeandidier E. Schluth C, et al. Among authors: jeandidier e. Am J Med Genet A. 2005 Jul 15;136(2):179-84. doi: 10.1002/ajmg.a.30745. Am J Med Genet A. 2005. PMID: 15940678 Review.
Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Groupe Français de Cytogénétique Hématologique.
Jeandidier E, Dastugue N, Mugneret F, Lafage-Pochitaloff M, Mozziconacci MJ, Herens C, Michaux L, Verellen-Dumoulin C, Talmant P, Cornillet-Lefebvre P, Luquet I, Charrin C, Barin C, Collonge-Rame MA, Pérot C, Van den Akker J, Grégoire MJ, Jonveaux P, Baranger L, Eclache-Saudreau V, Pagès MP, Cabrol C, Terré C, Berger R; Groupe Français de Cytogénétique Hématologique (GFCH). Jeandidier E, et al. Cancer Genet Cytogenet. 2006 Apr 1;166(1):1-11. doi: 10.1016/j.cancergencyto.2005.08.005. Cancer Genet Cytogenet. 2006. PMID: 16616106
A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity.
Jeandidier E, Gervais C, Radford-Weiss I, Zink E, Gangneux C, Eischen A, Galoisy AC, Helias C, Dano L, Cammarata O, Jung G, Harzallah I, Guérin E, Martzolff L, Drénou B, Lioure B, Tancrédi C, Rimelen V, Mauvieux L. Jeandidier E, et al. Cancer Genet. 2012 Jul-Aug;205(7-8):365-72. doi: 10.1016/j.cancergen.2012.04.007. Cancer Genet. 2012. PMID: 22867997
A Central Role of Telomere Dysfunction in the Formation of a Unique Translocation within the Sub-Telomere Region Resulting in Duplication and Partial Trisomy.
M'Kacher R, Miguet M, Maillard PY, Colicchio B, Scheidecker S, Najar W, Arnoux M, Oudrhiri N, Borie C, Biehler M, Plesch A, Heidingsfelder L, Bennaceur-Griscelli A, Dieterlen A, Voisin P, Junker S, Carde P, Jeandidier E. M'Kacher R, et al. Among authors: jeandidier e. Genes (Basel). 2022 Sep 29;13(10):1762. doi: 10.3390/genes13101762. Genes (Basel). 2022. PMID: 36292646 Free PMC article.
French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literature.
Luquet I, Mugneret F, Athis PD, Nadal N, Favre B, Abel C, Chelloug N, Lespinasse J, Portnoi MF, Joyé N, Dupont JM, Lebbar A, Bresson JL, Fellmann F, Siffroi JP, Chantot-Bastaraud S, Chiesa J, Amblard F, Devillard F, Jeandidier E, Boceno M, Rival JM, Bellec V, Lallaoui H, Delobel B, Croquette MF, Benzacken B. Luquet I, et al. Among authors: jeandidier e. Ann Genet. 2002 Apr-Jun;45(2):77-88. doi: 10.1016/s0003-3995(02)01118-8. Ann Genet. 2002. PMID: 12119216 Review.
Phenotype in X chromosome rearrangements: pitfalls of X inactivation study.
Schluth C, Cossée M, Girard-Lemaire F, Carelle N, Dollfus H, Jeandidier E, Flori E. Schluth C, et al. Among authors: jeandidier e. Pathol Biol (Paris). 2007 Feb;55(1):29-36. doi: 10.1016/j.patbio.2006.04.003. Epub 2006 May 11. Pathol Biol (Paris). 2007. PMID: 16690229
Therapy-related acute myeloid leukemia (t-AML) with poor-risk cytogenetics in two patients with persistent molecular complete remission of acute promyelocytic leukemia.
Ojeda-Uribe M, Schneider A, Luquet I, Berceanu A, Cornillet-Lefebvre P, Jeandidier E, Lioure B, Ades L, Mauvieux L, Himberlin C. Ojeda-Uribe M, et al. Among authors: jeandidier e. Eur J Haematol. 2012 Sep;89(3):267-72. doi: 10.1111/j.1600-0609.2012.01805.x. Epub 2012 Jun 27. Eur J Haematol. 2012. PMID: 22591288
44 results