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Leukemia & Lymphoma|November 8, 2001
A multicentric study of 41 cases of B-prolymphocytic leukemia: two evolutive formsC Hercher, M Robain, F Davi, et al.
Human Reproduction (Oxford, England)|July 8, 2011
Pregnancy outcomes in 188 French cases of prenatally diagnosed Klinefelter syndromeN Gruchy, F Vialard, M Decamp, et al.
Molecular Syndromology|October 30, 2013
Array-CGH Analysis Suggests Genetic Heterogeneity in RhombencephalosynapsisF Démurger, L Pasquier, C Dubourg, et al.
Journal of Medical Genetics|October 4, 2005
Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palateF Laumonnier, S Holbert, N Ronce, et al.
Cancer Genetics and Cytogenetics|June 19, 2007
Fluorescence in situ hybridization analysis of 110 hematopoietic disorders with chromosome 5 abnormalities: do de novo and therapy-related myelodysplastic syndrome-acute myeloid leukemia actually differ?M Lessard, C Hélias, S Struski, et al.
Clinical Genetics|October 13, 2009
Renal insufficiency, a frequent complication with age in oral-facial-digital syndrome type IS Saal, L Faivre, Bernard Aral, et al.
Prenatal Diagnosis|June 26, 2014
Pregnancy outcomes of prenatally diagnosed Turner syndrome: a French multicenter retrospective study including a series of 975 casesN Gruchy, F Vialard, E Blondeel, et al.
Annales De Genetique|July 18, 2002
French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literatureI Luquet, F Mugneret, P D Athis, et al.
Prenatal Diagnosis|January 8, 2014
A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomesJ Besseau-Ayasse, C Violle-Poirsier, A Bazin, et al.
Clinical Genetics|November 20, 2015
Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national surveyM Lefebvre, D Sanlaville, N Marle, et al.
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