Cornelia de Lange syndrome and cancer: An open question-Reference-Cited by-同舟云学术

Cornelia de Lange syndrome and cancer: An open question

Published:2022-10-17 Issue:1 Volume:191 Page:292-295
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:American J of Med Genetics Pt A

Author:

Pallotta Maria M.¹^ORCID,Di Nardo Maddalena¹^ORCID,Hennekam Raoul C. M.²,Kaiser Frank J.³⁴,Parenti Ilaria³,Pié Juan⁵,Ramos Feliciano J.⁵⁶,Kline Antonie D.⁷^ORCID,Musio Antonio¹^ORCID

Affiliation:

1. Institute for Biomedical Technologies National Research Council Pisa Italy

2. Department of Pediatrics, Emma Children's Hospital, Amsterdam UMC University of Amsterdam Amsterdam The Netherlands

3. Institute for Human Genetics University Hospital Essen, University of Duisburg‐Essen Essen Germany

4. Essen Center for Rare Diseases (Essener Zentrum für Seltene Erkrankungen, EZSE) University Hospital Essen Essen Germany

5. Unit of Clinical Genetics and Functional Genomics, Department of Pharmacology‐Physiology, School of Medicine University of Zaragoza, CIBERER‐GCV02 and ISS‐Aragon Zaragoza Spain

6. Clinical Genetics Unit, Service of Paediatrics University Hospital “Lozano Blesa”, University of Zaragoza, CIBERER GCV02 and ISS‐Aragón Zaragoza Spain

7. Harvey Institute for Human Genetics Greater Baltimore Medical Center Baltimore Maryland USA

Funder

Associazione Italiana per la Ricerca sul Cancro

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62992

Reference37 articles.

1. STAG2 loss rewires oncogenic and developmental programs to promote metastasis in Ewing sarcoma

2. Cornelia de Lange syndrome due to mosaic NIPBL mutation: antenatal presentation with sacrococcygeal teratoma

3. Barrett's esophagus;Bonino J. A.;Current Opinion in Gastroenterology,2006

4. Pediatric Pathology and Laboratory Medicine 17 2 Nephrogenic rests and renal abnormalities in Brachmann‐de Lange syndrome

5. Brachmann-Cornelia de Lange syndrome with a papilloma of the choroid plexus: analyses of molecular genetic characteristics of the patient and the tumor. A single-case study

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