Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication–deletion: Genotype–phenotype correlation for anomalies of the corpus callosum-Reference-Cited by-同舟云学术

Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication–deletion: Genotype–phenotype correlation for anomalies of the corpus callosum

Published:2021-12-15 Issue:3 Volume:101 Page:307-316
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Vibert Roseline¹^ORCID,Mignot Cyril¹,Keren Boris²,Chantot‐Bastaraud Sandra³,Portnoï Marie‐France³,Nouguès Marie‐Christine⁴,Moutard Marie‐Laure⁴,Faudet Anne¹,Whalen Sandra⁵,Haye Damien¹,Garel Catherine⁶,Chatron Nicolas⁷^ORCID,Rossi Massimiliano⁸,Vincent‐Delorme Catherine⁹,Boute Odile⁹,Delobel Bruno¹⁰,Andrieux Joris¹¹,Devillard Françoise¹²,Coutton Charles¹²^ORCID,Puechberty Jacques¹³^ORCID,Pebrel‐Richard Céline¹⁴,Colson Cindy¹⁵,Gerard Marion¹⁵,Missirian Chantal¹⁶,Sigaudy Sabine¹⁷,Busa Tiffany¹⁷,Doco‐Fenzy Martine¹⁸,Malan Valérie¹⁹,Rio Marlène²⁰,Doray Bérénice²¹,Sanlaville Damien⁷,Siffroi Jean‐Pierre³,Héron Delphine¹,Heide Solveig¹

Affiliation:

1. Département de Génétique, Hôpital Armand‐Trousseau and Groupe Hospitalier Pitié‐Salpêtrière, Centre de Référence Déficiences Intellectuelles de Causes Rares APHP‐Sorbonne Université Paris France

2. UF de Génomique du Développement, Département de Génétique, Groupe Hospitalier Pitié‐Salpêtrière APHP‐Sorbonne Université Paris France

3. Department of Cytogenetics, Armand Trousseau Hospital APHP‐Sorbonne Université Paris France

4. Service of Pediatric Neurology, Armand Trousseau Hospital APHP‐Sorbonne Université Paris France

5. UF de Génétique Clinique et Centre de Référence Maladies Rares des Anomalies du Développement et Syndromes Malformatifs, Hôpital Armand Trousseau, ERN ITHACA APHP‐Sorbonne Université Paris France

6. Department of Radiology, Armand Trousseau Hospital APHP‐Sorbonne Université Paris France

7. Departments of Genetics Lyon University Hospitals Lyon France

8. Genetics Department, Referral Centre for Developmental Abnormalities, Lyon University Hospital, and INSERM U1028, CNRS UMR5292, Lyon Neuroscience Research Centre, GENDEV Team Claude Bernard Lyon 1 University Bron France

9. Service of Clinical Genetic Jeanne de Flandre Hospital Lille France

10. Service of Cytogenetics Institut Catholique de Lille Lille France

11. Institute of Medical Genetics Jeanne de Flandre Hospital Lille France

12. Service de Génétique, Génomique, et Procréation, Centre Hospitalier Universitaire Grenoble Alpes, 38700 La Tronche, France; INSERM 1209, CNRS UMR 5309, Institute for Advanced Biosciences Université Grenoble Alpes Grenoble France

13. Department of Medical Genetics Arnaud de Villeneuve Hospital Montpellier France

14. Service of Cytogenetic Clermont‐Ferrand's University Hospital Clermont‐Ferrand France

15. Service of Clinical Genetic Caen's University Hospital Caen France

16. APHM, Laboratory of Genetic Timone Enfants' Hospital Marseille France

17. Department of Medical Genetics Timone Enfants' Hospital Marseille France

18. Genetic Department, AMH2 CHU Reims Reims France

19. APHP, Service de Médecine Génomique, Hôpital Necker‐Enfants Malades, Paris Université de Paris Paris France

20. Department of Genetics Hôpital Necker‐Enfants Malades, AP‐HP Paris France

21. Service of Genetic Felix Guyon Hospital La Réunion France

Publisher

Wiley

Subject