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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. Among authors: guerin e. Cancer Genet. 2012 Jul-Aug;205(7-8):365-72. doi: 10.1016/j.cancergen.2012.04.007. Cancer Genet. 2012. PMID: 22867997
Proximal 15q familial euchromatic variant and PWS/AS critical region duplication in the same patient: a cytogenetic pitfall.
Carelle-Calmels N, Girard-Lemaire F, Guérin E, Bieth E, Rudolf G, Biancalana V, Pecheur H, Demil H, Schneider T, de Saint-Martin A, Caron O, Legrain M, Gaston V, Flori E. Carelle-Calmels N, et al. Among authors: guerin e. Eur J Med Genet. 2008 Nov-Dec;51(6):547-57. doi: 10.1016/j.ejmg.2008.07.003. Epub 2008 Jul 22. Eur J Med Genet. 2008. PMID: 18692163
A compound heterozygote case of isolated sulfite oxidase deficiency.
Brumaru D, Guerin E, Voegeli AC, Eyer D, Maitre M. Brumaru D, et al. Among authors: guerin e. Mol Genet Metab Rep. 2017 Jul 6;12:99-102. doi: 10.1016/j.ymgmr.2017.06.009. eCollection 2017 Sep. Mol Genet Metab Rep. 2017. PMID: 28725568 Free PMC article.
203 results