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	1.	Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features. [electronic resource] by Haddad, Marie-Reine Mignon-Ravix, Cécile Cacciagli, Pierre Mégarbané, André Villard, Laurent Producer: 20091102 In: European journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A human interstitial telomere associates in vivo with specific TRF2 and TIN2 proteins. [electronic resource] by Mignon-Ravix, Cécile Depetris, Danielle Delobel, Bruno Croquette, Marie-Françoise Mattei, Marie-Geneviève Producer: 20020822 In: European journal of human genetics : EJHG vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Early-onset epileptic encephalopathy as the initial clinical presentation of WDR45 deletion in a male patient. [electronic resource] by Abidi, Affef Mignon-Ravix, Cécile Cacciagli, Pierre Girard, Nadine Milh, Mathieu Villard, Laurent Producer: 20161213 In: European journal of human genetics : EJHG vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Heterogeneity of FHF1 related phenotype: Novel case with early onset severe attacks of apnea, partial mitochondrial respiratory chain complex II deficiency, neonatal onset seizures without neurodegeneration. [electronic resource] by Villeneuve, Nathalie Abidi, Affef Cacciagli, Pierre Mignon-Ravix, Cécile Chabrol, Brigitte Villard, Laurent Milh, Mathieu Producer: 20180329 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	XNP-1/ATR-X acts with RB, HP1 and the NuRD complex during larval development in C. elegans. [electronic resource] by Cardoso, Carlos Couillault, Carole Mignon-Ravix, Cecile Millet, Anne Ewbank, Jonathan J Fontés, Michel Pujol, Nathalie Producer: 20050308 In: Developmental biology vol. 278 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	In human pachytene spermatocytes, SUMO protein is restricted to the constitutive heterochromatin. [electronic resource] by Metzler-Guillemain, Catherine Depetris, Danielle Luciani, Judith J Mignon-Ravix, Cecile Mitchell, Michael J Mattei, Marie-Genevieve Producer: 20081202 In: Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Mechanism of intrachromosomal triplications 15q11-q13: a new clinical report. [electronic resource] by Vialard, François Mignon-Ravix, Cécile Parain, Dominique Depetris, Danielle Portnoï, Marie-France Moirot, Hélène Mattei, Marie-Geneviève Producer: 20040106 In: American journal of medical genetics. Part A vol. 118A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Evidence that homozygous PTPRD gene microdeletion causes trigonocephaly, hearing loss, and intellectual disability. [electronic resource] by Choucair, Nancy Mignon-Ravix, Cecile Cacciagli, Pierre Abou Ghoch, Joelle Fawaz, Ali Mégarbané, André Villard, Laurent Chouery, Eliane Producer: 20150617 In: Molecular cytogenetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Disruption of the ATP8A2 gene in a patient with a t(10;13) de novo balanced translocation and a severe neurological phenotype. [electronic resource] by Cacciagli, Pierre Haddad, Marie-Reine Mignon-Ravix, Cécile El-Waly, Bilal Moncla, Anne Missirian, Chantal Chabrol, Brigitte Villard, Laurent Producer: 20110228 In: European journal of human genetics : EJHG vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Deletion of YWHAE in a patient with periventricular heterotopias and pronounced corpus callosum hypoplasia. [electronic resource] by Mignon-Ravix, Cécile Cacciagli, Pierre El-Waly, Bilal Moncla, Anne Milh, Mathieu Girard, Nadine Chabrol, Brigitte Philip, Nicole Villard, Laurent Producer: 20100506 In: Journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Subcellular distribution of HP1 proteins is altered in ICF syndrome. [electronic resource] by Luciani, Judith J Depetris, Danielle Missirian, Chantal Mignon-Ravix, Cécile Metzler-Guillemain, Catherine Megarbane, André Moncla, Anne Mattei, Marie-Geneviève Producer: 20050426 In: European journal of human genetics : EJHG vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Ambiguous genitalia, microcephaly, seizures, bone malformations, and early death: a distinct MCA/MR syndrome. [electronic resource] by Mégarbané, André Chouery, Eliane Mignon-Ravix, Cécile El Sabbagh, Sandra Corbani, Sandra Ghoch, Joelle Abou Jalkh, Nadine Mehawej, Cybel Lévy, Nicolas Villard, Laurent Producer: 20110801 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients. [electronic resource] by Choucair, Nancy Ghoch, Joelle Abou Corbani, Sandra Cacciagli, Pierre Mignon-Ravix, Cecile Salem, Nabiha Jalkh, Nadine El Sabbagh, Sandra Fawaz, Ali Ibrahim, Tony Villard, Laurent Mégarbané, André Chouery, Eliane Producer: 20150429 In: Molecular cytogenetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	PML nuclear bodies are highly organised DNA-protein structures with a function in heterochromatin remodelling at the G2 phase. [electronic resource] by Luciani, Judith J Depetris, Danielle Usson, Yves Metzler-Guillemain, Catherine Mignon-Ravix, Cecile Mitchell, Micheal J Megarbane, Andre Sarda, Pierre Sirma, Huseyin Moncla, Anne Feunteun, Jean Mattei, Marie-Genevieve Producer: 20061025 In: Journal of cell science vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Intragenic rearrangements in X-linked intellectual deficiency: results of a-CGH in a series of 54 patients and identification of TRPC5 and KLHL15 as potential XLID genes. [electronic resource] by Mignon-Ravix, Cécile Cacciagli, Pierre Choucair, Nancy Popovici, Cornel Missirian, Chantal Milh, Mathieu Mégarbané, André Busa, Tiffany Julia, Sophie Girard, Nadine Badens, Catherine Sigaudy, Sabine Philip, Nicole Villard, Laurent Producer: 20150331 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocations. [electronic resource] by Mignon-Ravix, Cécile Depetris, Danielle Luciani, Judith J Cuoco, Cristina Krajewska-Walasek, Malgorzata Missirian, Chantal Collignon, Patrick Delobel, Bruno Croquette, Marie-Françoise Moncla, Anne Kroisel, Peter M Mattei, Marie-Geneviève Producer: 20070622 In: European journal of human genetics : EJHG vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations. [electronic resource] by Milh, Mathieu Villeneuve, Nathalie Chouchane, Mondher Kaminska, Anna Laroche, Cécile Barthez, Marie Anne Gitiaux, Cyril Bartoli, Céline Borges-Correia, Ana Cacciagli, Pierre Mignon-Ravix, Cécile Cuberos, Hélène Chabrol, Brigitte Villard, Laurent Producer: 20111129 In: Epilepsia vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)