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Molecular Findings in Beckwith-Wiedemann Syndrome

American journal of medical genetics. Part C, Seminars in medical genetics, 2013-05, Vol.163C (2), p.131-140

2013

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Beckwith–Wiedemann syndrome: multiple molecular mechanisms

Expert reviews in molecular medicine, 2006-07, Vol.8 (17), p.1-19

2006

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Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith-Wiedemann Syndrome Cell Lines

International journal of molecular sciences, 2024-04, Vol.25 (7), p.3586

2024

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Diseases Predisposing to Adrenocortical Malignancy (Li–Fraumeni Syndrome, Beckwith–Wiedemann Syndrome, and Carney Complex)

Genetics of Endocrine Diseases and Syndromes, p.149-169

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S3570 Beckwith-Wiedemann Syndrome: A Rare Presentation of Chronic Portal Vein Thrombosis with Cavernous Transformation Extending to the Superior Mesenteric Vein

The American journal of gastroenterology, 2023-10, Vol.118 (10S), p.S2331-S2331

2023

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Beckwith-Wiedemann Syndrome Revisited

Human mutation, 2015-09, Vol.36 (9), p.iii-iii

Zander, Cecilia Soussi

2015

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Revisiting Wilms tumour surveillance in Beckwith-Wiedemann syndrome with IC2 methylation loss, reply

European journal of human genetics : EJHG, 2018-04, Vol.26 (4), p.471-472

2018

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Diffuse infantile hepatic hemangiomas in a patient with Beckwith–Wiedemann syndrome: A new association?

American journal of medical genetics. Part A, 2020-08, Vol.182 (8), p.1972-1976

2020

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Prevalence of (Epi)genetic Predisposing Factors in a 5-Year Unselected National Wilms Tumor Cohort: A Comprehensive Clinical and Genomic Characterization

Journal of clinical oncology, 2022-06, Vol.40 (17), p.1892-1902

2022

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BeckwithWiedemann Syndrome

Journal of Bangladesh College of Physicians & Surgeons, 2015-12, Vol.32 (3), p.167-170

2015

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Cutaneous Mucinosis Associated with Beckwith-Wiedemann Syndrome

Skinmed, 2020, Vol.18 (1), p.42-44

2020

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Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement

Nature reviews. Endocrinology, 2018-04, Vol.14 (4), p.229

2018

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EP09.32: Beckwith‐Wiedemann syndrome: a case report

Ultrasound in obstetrics & gynecology, 2015-09, Vol.46 (S1), p.222-222

2015

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P14.05: Early prenatal diagnosis of Beckwith‐Wiedemann syndrome

Ultrasound in obstetrics & gynecology, 2015-09, Vol.46 (S1), p.165-165

2015

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p57Kip2 knock-in mouse reveals CDK-independent contribution in the development of Beckwith-Wiedemann syndrome

The Journal of pathology, 2016-07, Vol.239 (3), p.250-261

2016

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Beckwith-Wiedemann syndrome associated with congenital cytomegalovirus in an HIV-exposed neonate

South African journal of obstetrics and gynaecology (1999), 2020-12, Vol.26 (2), p.79

2020

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Beckwith-Wiedemann syndrome in the two newborns

Journal of clinical neonatology, 2018-07, Vol.7 (3), p.162-165

2018

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EP24.18: Prenatal findings of Beckwith–Wiedemann syndrome

Ultrasound in obstetrics & gynecology, 2022-09, Vol.60 (S1), p.194-194

2022

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ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome

Nucleic acids research, 2005, Vol.33 (8), p.2650

2005

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Hepatocellular Carcinoma in a 24-Year-Old Female with Beckwith–Wiedemann Syndrome: A Case Report and Review of the Literature

Case reports in genetics, 2020-10, Vol.2020, p.8811296-4

2020

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Giant omphalocele and “prune belly” sequence as components of the Beckwith–Wiedemann syndrome

American journal of medical genetics, 2004-08, Vol.129A (2), p.198-200

2004

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Beckwith-Wiedemann syndrome mimicking the classical form of congenital adrenal hyperplasia in newborn screening

Archives of endocrinology and metabolism, 2024-02, Vol.68, p.e220395

2024

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534 Wnt/β-Catenin Activation in TGF-β Pathway ELF+/− , and ELF+/− / SMAD3+/− Mutant Mouse Models of Human Beckwith- Wiedemann Syndrome

Gastroenterology (New York, N.Y. 1943), 2008, Vol.134 (4), p.A-76-A-76

2008

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TGF-β/β2-spectrin/CTCF-regulated tumor suppression in human stem cell disorder Beckwith-Wiedemann syndrome

The Journal of clinical investigation, 2016-02, Vol.126 (2), p.527-542

2016

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A multidisciplinary approach to the treatment of oral manifestations associated with Beckwith-Wiedemann syndrome: a long-term case report

The Journal of the American Dental Association (1939), 2011-12, Vol.142 (12), p.1357

2011

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Molecular Findings in Beckwith-Wiedemann Syndrome

Beckwith–Wiedemann syndrome: multiple molecular mechanisms

Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith-Wiedemann Syndrome Cell Lines

Diseases Predisposing to Adrenocortical Malignancy (Li–Fraumeni Syndrome, Beckwith–Wiedemann Syndrome, and Carney Complex)

S3570 Beckwith-Wiedemann Syndrome: A Rare Presentation of Chronic Portal Vein Thrombosis with Cavernous Transformation Extending to the Superior Mesenteric Vein

Beckwith-Wiedemann Syndrome Revisited

Revisiting Wilms tumour surveillance in Beckwith-Wiedemann syndrome with IC2 methylation loss, reply

Diffuse infantile hepatic hemangiomas in a patient with Beckwith–Wiedemann syndrome: A new association?

Prevalence of (Epi)genetic Predisposing Factors in a 5-Year Unselected National Wilms Tumor Cohort: A Comprehensive Clinical and Genomic Characterization

BeckwithWiedemann Syndrome

Cutaneous Mucinosis Associated with Beckwith-Wiedemann Syndrome

Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement

EP09.32: Beckwith‐Wiedemann syndrome: a case report

P14.05: Early prenatal diagnosis of Beckwith‐Wiedemann syndrome

p57Kip2 knock-in mouse reveals CDK-independent contribution in the development of Beckwith-Wiedemann syndrome

Beckwith-Wiedemann syndrome associated with congenital cytomegalovirus in an HIV-exposed neonate

Beckwith-Wiedemann syndrome in the two newborns

EP24.18: Prenatal findings of Beckwith–Wiedemann syndrome

ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome

Hepatocellular Carcinoma in a 24-Year-Old Female with Beckwith–Wiedemann Syndrome: A Case Report and Review of the Literature

Giant omphalocele and “prune belly” sequence as components of the Beckwith–Wiedemann syndrome

Beckwith-Wiedemann syndrome mimicking the classical form of congenital adrenal hyperplasia in newborn screening

534 Wnt/β-Catenin Activation in TGF-β Pathway ELF+/− , and ELF+/− / SMAD3+/− Mutant Mouse Models of Human Beckwith- Wiedemann Syndrome

TGF-β/β2-spectrin/CTCF-regulated tumor suppression in human stem cell disorder Beckwith-Wiedemann syndrome

A multidisciplinary approach to the treatment of oral manifestations associated with Beckwith-Wiedemann syndrome: a long-term case report

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