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European Journal of Medical Genetics|May 21, 2009
Chromosome 22q13.3 deletion syndrome with a de novo interstitial 22q13.3 cryptic deletion disrupting SHANK3A Delahaye, A Toutain, A Aboura, et al.Prenatal Diagnosis|September 5, 2002
Female pseudohermaphroditism in a fetus with a deletion 9(q22.2q31.1)A Coulomb L'Herminé, A Aboura, B Simon-Bouy, et al.American Journal of Medical Genetics. Part A|November 5, 2004
De novo interstitial direct duplication of Xq21.1q25 associated with skewed X-inactivation patternG Tachdjian, A Aboura, M Benkhalifa, et al.Human Reproduction (Oxford, England)|April 23, 2005
Cytogenetic, molecular and testicular tissue studies in an infertile 45,X male carrying an unbalanced (Y;22) translocation: case reportS Brisset, V Izard, M Misrahi, et al.Prenatal Diagnosis|September 6, 2001
Cytogenetic analysis of trophoblasts by comparative genomic hybridization in embryo-fetal development anomaliesA C Tabet, A Aboura, M C Dauge, et al.American Journal of Medical Genetics. Part A|December 15, 2012
Maternal transmission of interstitial 8p23.1 deletion detected during prenatal diagnosisF Guimiot, C Dupont, A Fuentes-Duarte, et al.Human Reproduction (Oxford, England)|June 6, 2006
Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patientsM F Portnoï, A Aboura, G Tachdjian, et al.Clinical Genetics|May 11, 2011
3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndromeC Dupont, F Guimiot, L Perrin, et al.Journal of Medical Genetics|September 25, 2008
2q23.1 microdeletion identified by array comparative genomic hybridisation: an emerging phenotype with Angelman-like features?S Jaillard, C Dubourg, M Gérard-Blanluet, et al.Prenatal Diagnosis|February 3, 2007
Semilobar holoprosencephaly prenatal diagnosis: an unexpected complex rearrangement in a de novo apparently balanced reciprocal translocation on karyotypeS Kanafani, A Aboura, E Pipiras, et al.Pageof 3