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Cytogenetic and Genome Research|November 24, 2021
Intragenic Deletion of the ZMYND11 Gene in 10p15.3 is Associated with Developmental Delay Phenotype: A Case ReportMinh-Tuan Huynh, Cong Toai Tran, Madeleine Joubert, et al.Clinical Genetics|August 28, 2022
A Gardos channelopathy associated with nonimmune hydrops and fetal lossLeïla Ghesh, Thomas Besnard, Madeleine Joubert, et al.Journal of Pediatric Hematology/Oncology|April 9, 2015
Large Cell Neuroendocrine Carcinoma of the Nasopharynx: A Pediatric CaseClotilde Dumars, Estelle Thebaud, Madeleine Joubert, et al.Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|June 17, 2025
SOX2 Expression and Regulation in Pulmonary Aplasia/AgenesisAlexia Apostolou, Madeleine Joubert, Brice Poreau, et al.Archives of Surgery (Chicago, Ill. : 1960)|November 7, 2002
Intraductal papillary-mucinous tumors of the pancreas: predictive criteria of malignancy according to pathological examination of 53 casesPierre Bernard, Jean-Yves Scoazec, Madeleine Joubert, et al.Placenta|July 26, 2016
Perinatal prognosis of pregnancies complicated by placental chronic villitis or intervillositis of unknown etiology and combined lesions: About a series of 178 casesChristel Nowak, Madeleine Joubert, Frederique Jossic, et al.European Journal of Medical Genetics|November 28, 2020
Structural abnormalities of chromosome 8 and fetoplacental discrepancy: A second case report and review of fetal phenotype of 8p inverted duplication deletion syndromeMinh-Tuan Huynh, Anne-Sophie Riteau, Kamran Moradkhani, et al.American Journal of Medical Genetics. Part A|December 12, 2002
46,XY gonadal dysgenesis: evidence for autosomal dominant transmission in a large kindredCédric Le Caignec, Sabine Baron, Ken McElreavey, et al.Neurogenetics|June 16, 2021
Novel interstitial 2q12.3q13 microdeletion predisposes to developmental delay and behavioral problemsMinh-Tuan Huynh, Marion Gérard, Kara Ranguin, et al.American Journal of Medical Genetics. Part A|October 16, 2007
Complete sex reversal in a WAGR syndrome patientCedric Le Caignec, Capucine Delnatte, Joris R Vermeesch, et al.Pageof 4