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	1.	Stratum recruits Rab8 at Golgi exit sites to regulate the basolateral sorting of Notch and Sanpodo. [electronic resource] by Bellec, Karen Gicquel, Isabelle Le Borgne, Roland Producer: 20180731 In: Development (Cambridge, England) vol. 145 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Holoprosencephaly: An update on cytogenetic abnormalities. [electronic resource] by Bendavid, Claude Dupé, Valérie Rochard, Lucie Gicquel, Isabelle Dubourg, Christèle David, Véronique Producer: 20100304 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 154C Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos. [electronic resource] by Mercier, Sandra David, Véronique Ratié, Leslie Gicquel, Isabelle Odent, Sylvie Dupé, Valérie Producer: 20130911 In: Disease models & mechanisms vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Novel genes upregulated when NOTCH signalling is disrupted during hypothalamic development. [electronic resource] by Ratié, Leslie Ware, Michelle Barloy-Hubler, Frédérique Romé, Hélène Gicquel, Isabelle Dubourg, Christèle David, Véronique Dupé, Valérie Producer: 20140627 In: Neural development vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	MLPA screening reveals novel subtelomeric rearrangements in holoprosencephaly. [electronic resource] by Bendavid, Claude Dubourg, Christèle Pasquier, Laurent Gicquel, Isabelle Le Gallou, Simon Mottier, Stéphanie Durou, Marie-Renée Henry, Catherine Odent, Sylvie David, Véronique Producer: 20080128 In: Human mutation vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Phenotypic variability of a 4q34-->qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother. [electronic resource] by Bendavid, Claude Pasquier, Laurent Watrin, Tanguy Morcel, Karine Lucas, Josette Gicquel, Isabelle Dubourg, Christèle Henry, Catherine David, Véronique Odent, Sylvie Levêque, Jean Pellerin, Isabelle Guerrier, Daniel Producer: 20070322 In: European journal of medical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Molecular evaluation of foetuses with holoprosencephaly shows high incidence of microdeletions in the HPE genes. [electronic resource] by Bendavid, Claude Dubourg, Christèle Gicquel, Isabelle Pasquier, Laurent Saugier-Veber, Pascale Durou, Marie-Renée Jaillard, Sylvie Frébourg, Thierry Haddad, Bassem R Henry, Catherine Odent, Sylvie David, Véronique Producer: 20070402 In: Human genetics vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	NOTCH, a new signaling pathway implicated in holoprosencephaly. [electronic resource] by Dupé, Valérie Rochard, Lucie Mercier, Sandra Le Pétillon, Yann Gicquel, Isabelle Bendavid, Claude Bourrouillou, Georges Kini, Usha Thauvin-Robinet, Christel Bohan, Timothy P Odent, Sylvie Dubourg, Christèle David, Véronique Producer: 20110620 In: Human molecular genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Transcriptome variations in human CaCo-2 cells: a model for enterocyte differentiation and its link to iron absorption. [electronic resource] by Bédrine-Ferran, Hélène Le Meur, Nolwenn Gicquel, Isabelle Le Cunff, Martine Soriano, Nicolas Guisle, Isabelle Mottier, Stéphanie Monnier, Annabelle Teusan, Raluca Fergelot, Patricia Le Gall, Jean-Yves Léger, Jean Mosser, Jean Producer: 20041026 In: Genomics vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: an updated map of candidate loci. [electronic resource] by Bendavid, Claude Rochard, Lucie Dubourg, Christèle Seguin, Jonathan Gicquel, Isabelle Pasquier, Laurent Vigneron, Jaqueline Laquerrière, Annie Marcorelles, Pascale Jeanne-Pasquier, Corinne Rouleau, Caroline Jaillard, Sylvie Mosser, Jean Odent, Sylvie David, Veronique Producer: 20091022 In: Human mutation vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases. [electronic resource] by Mercier, Sandra Dubourg, Christèle Garcelon, Nicolas Campillo-Gimenez, Boris Gicquel, Isabelle Belleguic, Marion Ratié, Leslie Pasquier, Laurent Loget, Philippe Bendavid, Claude Jaillard, Sylvie Rochard, Lucie Quélin, Chloé Dupé, Valérie David, Véronique Odent, Sylvie Producer: 20120210 In: Journal of medical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)