Two new cases of interstitial 7q35q36.1 deletion including CNTNAP2 and KMT2C-Reference-Cited by-同舟云学术

Two new cases of interstitial 7q35q36.1 deletion including CNTNAP2 and KMT2C

Published:2021-09-28 Issue:11 Volume:9 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Tosca Lucie¹^ORCID,Drévillon Loïc¹,Mouka Aurélie¹,Lecerf Laure²³⁴,Briand Audrey²,Ortonne Valérie²,Benoit Virginie¹,Brisset Sophie¹,Van Maldergem Lionel⁵,Laudouar Quitterie⁶,Heide Solveig⁷,Goossens Michel²,Giurgea Irina⁸,Tachdjian Gérard¹,Métay Corinne²

Affiliation:

1. Service d'Histologie, Embryologie et Cytogénétique AP‐HP. Université Paris SaclayHôpital Antoine Béclère Clamart France

2. Service de Biochimie et Génétique AP‐HP. Hôpitaux Universitaires Henri MondorHôpital Henri Mondor Créteil France

3. Institut National de la Santé et de la Recherche MédicaleU955 Créteil France

4. Faculté de Médecine Université Paris‐Est Créteil France

5. Centre de Génétique Humaine Université de Franche‐Comté Besançon France

6. Service de Réanimation Néonatale AP‐HP. Université Paris SaclayHôpital Bicêtre Le Kremlin‐Bicêtre France

7. UF Génétique Clinique AP‐HP. Sorbonne UniversitéHôpital universitaire Pitié‐Salpêtrière Paris France

8. Département de Génétique Médicale INSERM Childhood Genetic DiseasesAP‐HP. Sorbonne UniversitéHôpital Trousseau Paris France

Funder

Ministère des Affaires Sociales et de la Santé

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1645

Reference23 articles.

1. Loss of Mll3 Catalytic Function Promotes Aberrant Myelopoiesis

2. Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestations

3. Long QT syndrome in chromosome 7q35q36.3 deletion involving KCNH2 gene: Warning for chlorpheniramine prescription

4. Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA

5. An interstitial deletion of chromosome 7(q35).

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