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Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome

Trends in genetics, 2008-04, Vol.24 (4), p.195-204

2008

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Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol

The Journal of pediatrics, 2016-09, Vol.176, p.142-149.e1

2016

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

European journal of medical genetics, 2016-01, Vol.59 (1), p.52-64

2016

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CDKN1C Mutations in HELLP/Preeclamptic Mothers of Beckwith–Wiedemann Syndrome (BWS) Patients

Placenta (Eastbourne), 2009-06, Vol.30 (6), p.551-554

2009

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Beckwith-Wiedemann Syndrome and IVF: A Case-Control Study

American journal of human genetics, 2004-09, Vol.75 (3), p.526-528

2004

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Evaluation of keyhole-pattern reduction glossoplasty for macroglossia in beckwith-wiedemann syndrome: A multidimensional analysis of postoperative course and outcomes

Journal of cranio-maxillo-facial surgery, 2024-05, Vol.52 (5), p.591-597

2024

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Prenatal diagnosis of paternal duplication of 11p15.5→14.3: Its implication of Beckwith–Wiedemann syndrome

Taiwanese journal of obstetrics & gynecology, 2016-12, Vol.55 (6), p.877-880

2016

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Associations between the timing of tongue reduction surgery, (Epi)genotype, and dentoskeletal development in patients with Beckwith-Wiedemann syndrome

Journal of cranio-maxillo-facial surgery, 2023-09, Vol.51 (9), p.568-573

2023

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Association of In Vitro Fertilization with Beckwith-Wiedemann Syndrome and Epigenetic Alterations of LIT1 and H19

American journal of human genetics, 2003-01, Vol.72 (1), p.156-160

2003

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Pancreatic surgery in infants with Beckwith–Wiedemann Syndrome and Hyperinsulinism

Journal of pediatric surgery, 2013-12, Vol.48 (12), p.2511-2516

2013

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Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

Trends in Genetics, 1997-08, Vol.13 (8), p.330-334

1997

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In Vitro Fertilization May Increase the Risk of Beckwith-Wiedemann Syndrome Related to the Abnormal Imprinting of the KCNQ1OT Gene

American journal of human genetics, 2003-05, Vol.72 (5), p.1338-1341

2003

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Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith–Wiedemann syndrome

Molecular genetics and metabolism, 2016-09, Vol.119 (1-2), p.8-13

2016

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Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith–Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer

Taiwanese journal of obstetrics & gynecology, 2014-03, Vol.53 (1), p.90-94

2014

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Long-term longitudinal evalutation of mandibular growth in patients with Beckwith-Wiedemann Syndrome treated and not treated with glossectomy

Journal of cranio-maxillo-facial surgery, 2020-12, Vol.48 (12), p.1126-1131

2020

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Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: A case series of 19 patients

Fertility and sterility, 2005-02, Vol.83 (2), p.349-354

2005

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CDKN1C mutations: two sides of the same coin

Trends in molecular medicine, 2014-11, Vol.20 (11), p.614-622

2014

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Taste and speech following surgical tongue reduction in children with Beckwith-Wiedemann syndrome

Journal of cranio-maxillo-facial surgery, 2016-06, Vol.44 (6), p.659-663

2016

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SNP arrays in Beckwith–Wiedemann syndrome: An improved diagnostic strategy

European journal of medical genetics, 2013-10, Vol.56 (10), p.546-550

2013

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The Clinical Course of an Overgrowth Syndrome, From Diagnosis in Infancy Through Adulthood: The Case of Beckwith–Wiedemann Syndrome

Current problems in pediatric and adolescent health care, 2015-04, Vol.45 (4), p.112-117

Pappas, John G., MD

2015

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First report of a successful pregnancy by preimplantation genetic testing for Beckwith-Wiedemann syndrome

Taiwanese journal of obstetrics & gynecology, 2022-01, Vol.61 (1), p.174-179

2022

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Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe

European journal of medical genetics, 2018-09, Vol.61 (9), p.499-507

2018

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Detection of hypermethylation at H19DMR at amniocentesis in a fetus with overgrowth, distended abdomen and Beckwith-Wiedemann syndrome

Taiwanese journal of obstetrics & gynecology, 2021-11, Vol.60 (6), p.1103-1106

2021

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Overgrowth Syndrome

The Veterinary clinics of North America. Food animal practice, 2019-07, Vol.35 (2), p.265-276

2019

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Epigenetic Alterations of H19 and LIT1 Distinguish Patients with Beckwith-Wiedemann Syndrome with Cancer and Birth Defects

American journal of human genetics, 2002-03, Vol.70 (3), p.604-611

2002

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Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome

Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol

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

CDKN1C Mutations in HELLP/Preeclamptic Mothers of Beckwith–Wiedemann Syndrome (BWS) Patients

Beckwith-Wiedemann Syndrome and IVF: A Case-Control Study

Evaluation of keyhole-pattern reduction glossoplasty for macroglossia in beckwith-wiedemann syndrome: A multidimensional analysis of postoperative course and outcomes

Prenatal diagnosis of paternal duplication of 11p15.5→14.3: Its implication of Beckwith–Wiedemann syndrome

Associations between the timing of tongue reduction surgery, (Epi)genotype, and dentoskeletal development in patients with Beckwith-Wiedemann syndrome

Association of In Vitro Fertilization with Beckwith-Wiedemann Syndrome and Epigenetic Alterations of LIT1 and H19

Pancreatic surgery in infants with Beckwith–Wiedemann Syndrome and Hyperinsulinism

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

In Vitro Fertilization May Increase the Risk of Beckwith-Wiedemann Syndrome Related to the Abnormal Imprinting of the KCNQ1OT Gene

Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith–Wiedemann syndrome

Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith–Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer

Long-term longitudinal evalutation of mandibular growth in patients with Beckwith-Wiedemann Syndrome treated and not treated with glossectomy

Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: A case series of 19 patients

CDKN1C mutations: two sides of the same coin

Taste and speech following surgical tongue reduction in children with Beckwith-Wiedemann syndrome

SNP arrays in Beckwith–Wiedemann syndrome: An improved diagnostic strategy

The Clinical Course of an Overgrowth Syndrome, From Diagnosis in Infancy Through Adulthood: The Case of Beckwith–Wiedemann Syndrome

First report of a successful pregnancy by preimplantation genetic testing for Beckwith-Wiedemann syndrome

Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe

Detection of hypermethylation at H19DMR at amniocentesis in a fetus with overgrowth, distended abdomen and Beckwith-Wiedemann syndrome

Overgrowth Syndrome

Epigenetic Alterations of H19 and LIT1 Distinguish Patients with Beckwith-Wiedemann Syndrome with Cancer and Birth Defects

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