Morgane Stichelbout

Blepharocheilodontic syndrome is a CDH1 pathway–related disorder due to mutations in CDH1 and CTNND1

Jamal Ghoumid, Morgane Stichelbout, Anne‐Sophie Jourdain et al. · Genetics in Medicine · 2017 · 68 citations · Full text

Blepharocheilodontic Syndrome, Pathology, Molecular Medicine +2

SALL4 expression in gestational trophoblastic tumors: a useful tool to distinguish choriocarcinoma from placental site trophoblastic tumor and epithelioid trophoblastic tumor

Morgane Stichelbout, Louise Devisme, Hélène Franquet‐Ansart et al. · Human Pathology · 2016 · 61 citations

Developmental Biology, Epithelioid Trophoblastic Tumor, Placental Development +8

Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome

Carine Bonnard, Mohammad Shboul, Seyed Hassan Tonekaboni et al. · European Journal of Medical Genetics · 2018 · 36 citations

Ciliopathy-associated Gene Cplane1, Joubert Syndrome, Genetic Disorder +8

Perinatal outcome of placental massive perivillous fibrin deposition: a case–control study

Louise Devisme, Claire Chauvière, Hélène Franquet‐Ansart et al. · Prenatal Diagnosis · 2017 · 29 citations

Reproductive Sciences, Reproductive Health, Fetal Medicine +26

<i>COL4A1/COL4A2</i> and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage

Thibault Coste, Catherine Vincent‐Delorme, Morgane Stichelbout et al. · Prenatal Diagnosis · 2022 · 22 citations · Full text