Corpus Callosum Abnormalities and Short Femurs in Beckwith–Wiedemann Syndrome: A Report of Two Fetal Cases-Reference-Cited by-同舟云学术

Corpus Callosum Abnormalities and Short Femurs in Beckwith–Wiedemann Syndrome: A Report of Two Fetal Cases

Published:2018-11-02 Issue:6 Volume:37 Page:411-417
ISSN:1551-3815
Container-title:Fetal and Pediatric Pathology
language:en
Short-container-title:Fetal and Pediatric Pathology

Author:

Beaufrère Aurélie¹,Bonnière Maryse¹,Tantau Julia²,Roth Philippe³,Schaerer Elodie²,Brioude Fréderic⁴,Netchine Irène⁴,Bessières Bettina¹,Gelot Antoinette⁵,Vekemans Michel¹,Razavi Ferechté¹,Heron Delphine²,Attié-Bitach Tania¹⁶

Affiliation:

1. Unité d’Embryofœtopathologie, Service d'Histologie-Embryologie-Cytogénétique, Hôpital Necker-Enfants Malades, APHP, Paris, France;

2. Département de Génétique Médicale, Hôpital Trousseau, APHP, Paris, France;

3. Service de Gynécologie-Obstétrique, Hôpital Necker-Enfants Malades, APHP, Paris, France;

4. Service d'Explorations Fonctionnelles Endocriniennes, Hôpital Trousseau, APHP, Paris, France;

5. Service d'Anatomie et Cytologie Pathologiques, Hôpital Trousseau, APHP, Paris, France;

6. INSERM U1163, Institut Imagine, Université Paris Descartes, Paris, France

Publisher

Informa UK Limited

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology, and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/15513815.2018.1520942

Reference18 articles.

1. Recommendations of the Scientific Committee of the Italian Beckwith–Wiedemann Syndrome Association on the diagnosis, management and follow-up of the syndrome

2. Clinical and molecular analyses of Beckwith-Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniques

3. (Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: a paradigm for genomic medicine

4. Epigenetic and genetic alterations of the imprinting disorder Beckwith–Wiedemann syndrome and related disorders

5. Beckwith-Wiedemann syndrome

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