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Fetal Description of the Pancreatic Agenesis and Holoprosencephaly Syndrome Associated to a Specific CNOT1 Variant.
Cospain, Auriane; Faoucher, Marie; Cauchois, Aurélie; Carre, Wilfrid; Quelin, Chloé; Dubourg, Christèle.
Affiliation
  • Cospain A; Service de Génétique Clinique, Centre de Référence Maladies Rares CLAD-Ouest, ERN ITHACA, Hôpital Sud, 36684CHU Rennes, Rennes, France.
  • Faoucher M; Service de Génétique Moléculaire et Génomique, 36684CHU, Rennes, France.
  • Cauchois A; Service de Génétique Moléculaire et Génomique, 36684CHU, Rennes, France.
  • Carre W; CNRS, IGDR, UMR 6290, Univ Rennes, Rennes, France.
  • Quelin C; Anatomie et cytologie pathologiques, CHU de Rennes, Rennes, France.
  • Dubourg C; Service de Génétique Moléculaire et Génomique, 36684CHU, Rennes, France.
Pediatr Dev Pathol ; 25(5): 548-552, 2022.
Article in En | MEDLINE | ID: mdl-35481434
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Holoprosencephaly Type of study: Diagnostic_studies / Risk_factors_studies Limits: Female / Humans / Pregnancy Language: En Journal: Pediatr Dev Pathol Year: 2022 Document type: Article
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Holoprosencephaly Type of study: Diagnostic_studies / Risk_factors_studies Limits: Female / Humans / Pregnancy Language: En Journal: Pediatr Dev Pathol Year: 2022 Document type: Article