Roles of Wnt pathway genes wls , wnt9a , wnt5b, frzb and gpc4 in regulating convergent-extension during palate morphogenesis
Rochard, Lucie, Monica, Stefanie D., Ling, Irving T. C., Kong, Yawei, Roberson, Sara, Harland, Richard, Halpern, Marnie, Liao, Eric C.
Published in Development (Cambridge) (01.01.2016)
Published in Development (Cambridge) (01.01.2016)
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Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci
Morcel, Karine, Watrin, Tanguy, Pasquier, Laurent, Rochard, Lucie, Le Caignec, Cédric, Dubourg, Christèle, Loget, Philippe, Paniel, Bernard-Jean, Odent, Sylvie, David, Véronique, Pellerin, Isabelle, Bendavid, Claude, Guerrier, Daniel
Published in Orphanet journal of rare diseases (15.03.2011)
Published in Orphanet journal of rare diseases (15.03.2011)
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Roles of Wnt pathway genes wls, wnt9a, wnt5b, frzb and gpc4 in regulating convergent-extension during zebrafish palate morphogenesis
Rochard, Lucie, Monica, Stefanie D, Ling, Irving T C, Kong, Yawei, Roberson, Sara, Harland, Richard, Halpern, Marnie, Liao, Eric C
Published in Development (Cambridge) (15.07.2016)
Published in Development (Cambridge) (15.07.2016)
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Requirement for frzb and fzd7a in cranial neural crest convergence and extension mechanisms during zebrafish palate and jaw morphogenesis
Kamel, George, Hoyos, Tatiana, Rochard, Lucie, Dougherty, Max, Kong, Yawei, Tse, William, Shubinets, Valeriy, Grimaldi, Michael, Liao, Eric C.
Published in Developmental biology (15.09.2013)
Published in Developmental biology (15.09.2013)
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Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: An updated map of candidate loci
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
Published in Human mutation (01.08.2009)
Published in Human mutation (01.08.2009)
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New findings for phenotype–genotype correlations in a large European series of holoprosencephaly cases
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
Published in Journal of medical genetics (01.11.2011)
Published in Journal of medical genetics (01.11.2011)
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Holoprosencephaly: An update on cytogenetic abnormalities: holoprosencephaly and cytogenetics
Bendavid, Claude, Dupé, Valérie, Rochard, Lucie, Gicquel, Isabelle, Dubourg, Christèle, David, Véronique
Published in American journal of medical genetics. Part C, Seminars in medical genetics (15.02.2010)
Published in American journal of medical genetics. Part C, Seminars in medical genetics (15.02.2010)
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Holoprosencephaly: An Update on Cytogenetic Abnormalities: Holoprosencephaly
BENDAVID, Claude, DUPE, Valérie, ROCHARD, Lucie, GICQUEL, Isabelle, DUBOURG, Christèle, DAVID, Véronique
Published in American journal of medical genetics. Part C, Seminars in medical genetics (2010)
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Published in American journal of medical genetics. Part C, Seminars in medical genetics (2010)
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NOTCH, a new signaling pathway implicated in holoprosencephaly
DUPE, Valérie, ROCHARD, Lucie, ODENT, Sylvie, DUBOURG, Christèle, DAVID, Veronique, MERCIER, Sandra, LE PETILLON, Yann, GICQUEL, Isabelle, BENDAVID, Claude, BOURROUILLOU, Georges, KINI, Usha, THAUVIN-ROBINET, Christel, BOHAN, Timothy P
Published in Human molecular genetics (15.03.2011)
Published in Human molecular genetics (15.03.2011)
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Utero-vaginal aplasia
Morcel, Karine, Watrin, Tanguy, Pasquier, Laurent, Rochard, Lucie, Le Caignec, Cédric, Dubourg, Christèle, Loget, Philippe, Paniel, Bernard-Jean, Odent, Sylvie, David, Véronique, Pellerin, Isabelle, Bendavid, Claude, Guerrier, Daniel
Published in Orphanet journal of rare diseases (15.03.2011)
Published in Orphanet journal of rare diseases (15.03.2011)
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