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Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 1, 2006
An association of pleuropulmonary blastoma and cystic nephroma: possible genetic associationDorotheé Bouron-Dal Soglio, Isabelle Harvey, Salam Yazbeck, et al.AJR. American Journal of Roentgenology|February 21, 2004
Complementary role of MRI after sonography in assessing bilateral urinary tract anomalies in the fetusMarie Cassart, Anne Massez, Thierry Metens, et al.Fetal Diagnosis and Therapy|June 28, 2005
Prenatal diagnosis of cloverleaf skull: watch the hands!Guillaume Gorincour, Françoise Rypens, Andrée Grignon, et al.Journal of Perinatal Medicine|February 8, 2020
Prenatal findings, neonatal symptoms and neurodevelopmental outcome of congenital cytomegalovirus infection in a university hospital in Montreal, QuebecAnne-Frédérique Minsart, Françoise Rypens, Mina Smiljkovic, et al.BMC Neurology|September 3, 2020
A case report of severe tuberous sclerosis complex detected in utero and linked to a novel duplication in the TSC2 geneValérie Mongrain, Nicolaas H van Doesburg, Françoise Rypens, et al.The American Journal of Surgical Pathology|June 4, 2008
Chondroid cystic malformation of the lung with trisomy 8 mosaicism: a new cystic lung malformationDorothée Bouron-Dal Soglio, Anne-Laure Rougemont, Anthony S De Buys Roessingh, et al.Pediatric Radiology|April 27, 2004
Fetal hydronephrosis: is there hope for consensus?Sanna Toiviainen-Salo, Laurent Garel, Andrée Grignon, et al.American Journal of Medical Genetics. Part A|December 28, 2019
Retrospective analysis of fetal vertebral defects: Associated anomalies, etiologies, and outcomeGabrielle T Lemire, Éliane Beauregard-Lacroix, Philippe M Campeau, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 26, 2017
A Novel PGM3 Mutation Is Associated With a Severe Phenotype of Bone Marrow Failure, Severe Combined Immunodeficiency, Skeletal Dysplasia, and Congenital MalformationsGuillermo Pacheco-Cuéllar, Julie Gauthier, Valérie Désilets, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesisSarah Boissel, Catherine Fallet-Bianco, David Chitayat, et al.Pageof 4