Genome-Wide Paternal Uniparental Disomy as a Cause of Beckwith-Wiedemann Syndrome Associated with Recurrent Virilizing Adrenocortical Tumors-Reference-Cited by-同舟云学术

Genome-Wide Paternal Uniparental Disomy as a Cause of Beckwith-Wiedemann Syndrome Associated with Recurrent Virilizing Adrenocortical Tumors

Published:2014-11-03 Issue:07 Volume:47 Page:497-503
ISSN:0018-5043
Container-title:Hormone and Metabolic Research
language:en
Short-container-title:Horm Metab Res

Author:

Bertoin F.¹,Letouzé E.²,Grignani P.³,Patey M.⁴,Rossignol S.⁵,Libé R.⁶,Pasqual C.⁷,Lardière-Deguelte S.⁸,Hoeffel-Fornes C.⁹,Gaillard D.¹⁰,Previderè C.³,Delemer B.¹,Lalli E.¹¹

Affiliation:

1. Department of Endocrinology, CHU Reims, Hôpital Robert Debré, Reims, France

2. Programme Cartes d’Identité des Tumeurs, Ligue Nationale contre le Cancer, Paris, France

3. Department of Public Health, Experimental and Forensic Medicine, University of Pavia, Pavia, Italy

4. Department of Pathology, CHU Reims, Hôpital Robert Debré, Reims, France

5. Laboratory of Endocrine Functional Explorations, APHP, Hôpital Armand Trousseau, INSERM UMRS 938 Team 4, Université Pierre et Marie Curie-Paris, Faculté de Médecine, Paris, France

6. Department of Endocrinology-Metabolism-Cancer, APHP, Institut Cochin, Université Paris V-René Descartes, Paris, France

7. Service of Diabetology, Hospital of Troyes, Troyes, France

8. Department of Endocrine Surgery, CHU Reims, Hôpital Robert Debré, Reims, France

9. Department of Radiology, CHU Reims, Hôpital Robert Debré, Reims, France

10. Department of Genetics, CHU Reims, Hôpital Robert Debré, Reims, France

11. Institut de Pharmacologie Moléculaire et Cellulaire, CNRS UMR7275, Sophia Antipolis-Valbonne, France

Publisher

Georg Thieme Verlag KG

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,General Medicine,Endocrinology, Diabetes and Metabolism

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0034-1394371.pdf

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4. Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge;European Journal of Human Genetics;2022-07-27

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