Placental Pathology in Beckwith–Wiedemann Syndrome According to Genotype/Epigenotype Subgroups
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Title
Placental Pathology in Beckwith–Wiedemann Syndrome According to Genotype/Epigenotype Subgroups
Authors
Keywords
-
Journal
Fetal and Pediatric Pathology
Volume -, Issue -, Pages 1-13
Publisher
Informa UK Limited
Online
2019-01-12
DOI
10.1080/15513815.2018.1504842
References
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Related references
Note: Only part of the references are listed.- Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement
- (2018) Frédéric Brioude et al. Nature Reviews Endocrinology
- Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups
- (2016) Saskia M. Maas et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Fetal growth patterns in Beckwith-Wiedemann syndrome
- (2016) A. Mussa et al. CLINICAL GENETICS
- Genomic imprinting in the human placenta
- (2015) David Monk AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY
- Classification of placental lesions
- (2015) Raymond W. Redline AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY
- Mutations of the ImprintedCDKN1CGene as a Cause of the Overgrowth Beckwith-Wiedemann Syndrome: Clinical Spectrum and Functional Characterization
- (2015) Frederic Brioude et al. HUMAN MUTATION
- Placental Mesenchymal Dysplasia without Fetal Development in a Twin Gestation: A Case Report and Review of the Spectrum of Androgenetic Biparental Mosaicism
- (2015) Rebecca L. Linn et al. PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
- Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects
- (2014) Abdulla Ibrahim et al. Clinical Epigenetics
- Beckwith-Wiedemann Syndrome: Growth Pattern and Tumor Risk according to Molecular Mechanism, and Guidelines for Tumor Surveillance
- (2013) F. Brioude et al. Hormone Research in Paediatrics
- Characterization of Androgenetic/Biparental Mosaic/Chimeric Conceptions, Including Those With a Molar Component
- (2013) Gloria H. Lewis et al. INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY
- Characteristics of hydatidiform moles: analysis of a prospective series with p57 immunohistochemistry and molecular genotyping
- (2013) Natalie Banet et al. MODERN PATHOLOGY
- Making big cells: One size does not fit all
- (2013) B. R. Calvi PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The placenta in Beckwith-Wiedemann syndrome: genotype-phenotype associations, excessive extravillous trophoblast and placental mesenchymal dysplasia
- (2012) Jane E. Armes et al. PATHOLOGY
- The hallmarks of CDKN1C (p57, KIP2) in cancer
- (2011) Edel Kavanagh et al. BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER
- Beckwith-Wiedemann syndrome with placental chorangioma due to H19-differentially methylated region hypermethylation: A case report
- (2011) Aiko Aoki et al. JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH
- Clinical features and natural history of Beckwith-Wiedemann syndrome: presentation of 74 new cases
- (2010) Margaret Elliott et al. CLINICAL GENETICS
- Beckwith–Wiedemann syndrome
- (2009) Rosanna Weksberg et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- IMMUNOHISTOCHEMICAL EXPRESSION OF P57 IN PLACENTAL VASCULAR PROLIFERATIVE DISORDERS OF PRETERM AND TERM PLACENTAS
- (2009) Fabienne Allias et al. Fetal and Pediatric Pathology
- Insulin and the IGF system in the human placenta of normal and diabetic pregnancies
- (2009) Ursula Hiden et al. JOURNAL OF ANATOMY
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