₄Catherine Fallet-Bianco

Catherine Fallet-Bianco Articles (4) [selected PubMed articles for the year 2007 with the links to a full text at PubMed]

• Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A). (2007) >>

  Institut Cochin, Université Paris Descartes, Centre national de la recherche scientifique Unité Mixte de Recherche 8104, Paris, France.

  ₂Bahi, Nadia, ₂Francis, Fiona, ₁₂Toutain, Annick, ₄Pasquier, Laurent, ₂Ville, Dorothée, ₇Harvey, Robert J, ₈Flint, Jonathan, ₂Joriot, Sylvie, ₅Bienvenu, Thierry, ₃Desguerre, Isabelle, ₃Poirier, Karine, ₃Saillour, Yoann, ₂₂Fryns, Jean-Pierre, ₂Goldenberg, Alice, ₆Siebold, Christian, ₅Odent, Sylvie, ₅Keays, David A, ₃Moutard, Marie-Laure, ₁₃Chelly, Jamel, ₁Tuy, Françoise Phan Dinh, ₃Beldjord, Cherif, ₄Fallet-Bianco, Catherine, ₁Manouvrier, Sylvie, ₈Van Esch, Hilde.

• Isolated posterior cerebellar vermal defect: a morphological study of midsagittal cerebellar vermis in 4 fetuses--early stage of Dandy-Walker continuum or new vermal dysgenesis? (2007) >>

  Department of Pathology, Hospital S. Giovanni di Dio, e Ruggi d'Aragona, Salerno, Italy.

  ₄Fallet-Bianco, Catherine, ₁Russo, Rosa.

• Matthew-Wood syndrome: report of two new cases supporting autosomal recessive inheritance and exclusion of FGF10 and FGFR2. (2007) >>

  Assistance Publique - Hôpitaux de Paris, Hôpital Necker - Enfants Malades, Department of Genetics, Embryo-Fetal Pathology Unit, Paris, France.

  ₃Golzio, Christelle, ₄Benachi, Alexandra, ₁Morichon, Nicole, ₂Martinovic-Bouriel, Jelena, ₁Aubry, Marie-Cécile, ₄Malan, Valérie, ₂Bonniere, Maryse, ₁Mirlesse, Véronique, ₁Bernabé-Dupont, Céline, ₂Grattagliano-Bessières, Bettina, ₃Esculpavit, Chantal, ₁₀Encha-Razavi, Ferechte, ₄Fallet-Bianco, Catherine, ₁Etchevers, Heather, ₁₀Attié-Bitach, Tania, ₁₁Vekemans, Michel, ₂Le Bidois, Jérôme.

• Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency. (2007) >>

  Département de Génétique et Développement, Institut Cochin, F-75014 Paris, France.

  ₂Francis, Fiona, ₁Souville, Isabelle, ₂Pinard, Jean-Marc, ₃Saillour, Yoann, ₄Meyer, Gundela, ₆Dhenain, Marc, ₁Kappeler, Caroline, ₁₃Chelly, Jamel, ₃Beldjord, Cherif, ₁₀Encha-Razavi, Ferechte, ₄Fallet-Bianco, Catherine, ₄Souil, Evelyne, ₂Marty, Serge, ₁Phan Dinh Tuy, Françoise, ₃Volk, Andreas.