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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: girard lemaire f. 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
Genetic compensation in a human genomic disorder.
Carelle-Calmels N, Saugier-Veber P, Girard-Lemaire F, Rudolf G, Doray B, Guérin E, Kuhn P, Arrivé M, Gilch C, Schmitt E, Fehrenbach S, Schnebelen A, Frébourg T, Flori E. Carelle-Calmels N, et al. Among authors: girard lemaire f. N Engl J Med. 2009 Mar 19;360(12):1211-6. doi: 10.1056/NEJMoa0806544. N Engl J Med. 2009. PMID: 19297573 Free article.
Gastrointestinal stromal tumor in an XYY/XY male.
Limacher JM, Girard-Lemaire F, Jeandidier E, Chenard-Neu MP, Kassem M, Flori E, Bergerat JP. Limacher JM, et al. Cancer Genet Cytogenet. 2002 Mar;133(2):152-5. doi: 10.1016/s0165-4608(01)00566-0. Cancer Genet Cytogenet. 2002. PMID: 11943343 Review.
Prenatal sonographic diagnosis of the 49,XXXXY syndrome.
Schluth C, Doray B, Girard-Lemaire F, Kohler M, Langer B, Gasser B, Lindner V, Flori E. Schluth C, et al. Prenat Diagn. 2002 Dec;22(13):1177-80. doi: 10.1002/pd.473. Prenat Diagn. 2002. PMID: 12478628 Review.
18 results