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Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith–Wiedemann syndrome

Journal of medical genetics, 2016-01, Vol.53 (1), p.53-61

2016

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Development of disease-specific growth charts for Korean children with Beckwith-Wiedemann syndrome

Clinical genetics, 2024-05, Vol.105 (5), p.533-542

2024

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Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

Journal of medical genetics, 2003-01, Vol.40 (1), p.62-64

2003

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Beckwith–Wiedemann syndrome

International journal of oral and maxillofacial surgery, 2019-12, Vol.48 (12), p.1606-1607

Schendel, S.A.

2019

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Beckwith-Wiedemann syndrome

The Pan African medical journal, 2023, Vol.45, p.17-17

2023

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Tumor screening in Beckwith-Wiedemann syndrome-To screen or not to screen?

American journal of medical genetics. Part A, 2016-09, Vol.170A (9), p.2261-2264

2016

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Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith―Wiedemann syndrome and Silver―Russell syndrome

Human molecular genetics, 2011-04, Vol.20 (7), p.1363-1374

2011

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Large offspring syndrome: A bovine model for the human loss-of-imprinting overgrowth syndrome Beckwith-Wiedemann

Epigenetics, 2013-06, Vol.8 (6), p.591-601

2013

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The utility of alpha‐fetoprotein screening in Beckwith–Wiedemann syndrome

American journal of medical genetics. Part A, 2017-03, Vol.173 (3), p.581-584

2017

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Kagami‐Ogata syndrome: an important differential diagnosis to Beckwith‐Wiedemann syndrome

Journal of clinical ultrasound, 2020-05, Vol.48 (4), p.240-243

2020

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Pediatric chondrodermatitis nodularis helicis (CNH) in a child with Beckwith‐Wiedemann syndrome (BWS)

Pediatric dermatology, 2019-05, Vol.36 (3), p.388-390

2019

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p57(Kip2) 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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Serum alpha‐fetoprotein screening for hepatoblastoma in Beckwith–Wiedemann syndrome

American journal of medical genetics. Part A, 2017-03, Vol.173 (3), p.585-587

2017

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Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type Ib in a patient with multilocus imprinting disturbance: a female-dominant phenomenon?

Journal of human genetics, 2016-08, Vol.61 (8), p.765-769

2016

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Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome

Journal of medical genetics, 2003-11, Vol.40 (11), p.797-801

2003

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Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome

Pediatrics (Evanston), 2017-07, Vol.140 (1)

2017

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Epigenetic Silencing of β-Spectrin, a TGF-β Signaling/Scaffolding Protein in a Human Cancer Stem Cell Disorder: BECKWITH-WIEDEMANN SYNDROME

The Journal of biological chemistry, 2010-11, Vol.285 (46), p.36112-36120

2010

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Prenatally diagnosed omphaloceles: Report of 92 cases and association with Beckwith‐Wiedemann syndrome

Prenatal diagnosis, 2021-06, Vol.41 (7), p.798-816

2021

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Longitudinal Monitoring of Alpha-Fetoprotein by Dried Blood Spot for Hepatoblastoma Screening in Beckwith⁻Wiedemann Syndrome

Cancers, 2019-01, Vol.11 (1), p.86

2019

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Fetal growth patterns in Beckwith-Wiedemann syndrome

Clinical genetics, 2016-07, Vol.90 (1), p.21-27

2016

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Prenatal imaging throughout gestation in Beckwith‐Wiedemann syndrome

Prenatal diagnosis, 2019-08, Vol.39 (9), p.792-795

2019

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(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome

Molecular genetics & genomic medicine, 2020-09, Vol.8 (9), p.e1386-n/a

2020

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Beckwith–Wiedemann syndrome in diverse populations

American journal of medical genetics. Part A, 2019-04, Vol.179 (4), p.525-533

2019

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Familial Beckwith‐Wiedemann syndrome in a multigenerational family: Forty years of careful phenotyping

American journal of medical genetics. Part A, 2023-02, Vol.191 (2), p.348-356

2023

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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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Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith–Wiedemann syndrome

Development of disease-specific growth charts for Korean children with Beckwith-Wiedemann syndrome

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

Beckwith–Wiedemann syndrome

Beckwith-Wiedemann syndrome

Tumor screening in Beckwith-Wiedemann syndrome-To screen or not to screen?

Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith―Wiedemann syndrome and Silver―Russell syndrome

Large offspring syndrome: A bovine model for the human loss-of-imprinting overgrowth syndrome Beckwith-Wiedemann

The utility of alpha‐fetoprotein screening in Beckwith–Wiedemann syndrome

Kagami‐Ogata syndrome: an important differential diagnosis to Beckwith‐Wiedemann syndrome

Pediatric chondrodermatitis nodularis helicis (CNH) in a child with Beckwith‐Wiedemann syndrome (BWS)

p57(Kip2) knock-in mouse reveals CDK-independent contribution in the development of Beckwith-Wiedemann syndrome

Serum alpha‐fetoprotein screening for hepatoblastoma in Beckwith–Wiedemann syndrome

Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type Ib in a patient with multilocus imprinting disturbance: a female-dominant phenomenon?

Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome

Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome

Epigenetic Silencing of β-Spectrin, a TGF-β Signaling/Scaffolding Protein in a Human Cancer Stem Cell Disorder: BECKWITH-WIEDEMANN SYNDROME

Prenatally diagnosed omphaloceles: Report of 92 cases and association with Beckwith‐Wiedemann syndrome

Longitudinal Monitoring of Alpha-Fetoprotein by Dried Blood Spot for Hepatoblastoma Screening in Beckwith⁻Wiedemann Syndrome

Fetal growth patterns in Beckwith-Wiedemann syndrome

Prenatal imaging throughout gestation in Beckwith‐Wiedemann syndrome

(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome

Beckwith–Wiedemann syndrome in diverse populations

Familial Beckwith‐Wiedemann syndrome in a multigenerational family: Forty years of careful phenotyping

Beckwith–Wiedemann syndrome: multiple molecular mechanisms

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