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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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Altered microRNA expression profiles in large offspring syndrome and Beckwith-Wiedemann syndrome

Epigenetics, 2019-09, Vol.14 (9), p.850-876

2019

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Beckwith-Wiedemann Syndrome, Delayed Abdominal Wall Closure, and Neonatal Intussusception -Case Report and Literature Review

Fetal and pediatric pathology, 2012-12, Vol.31 (6), p.448-452

2012

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Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi

Epigenetics, 2015-07, Vol.10 (7), p.643-649

2015

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Placental Pathology in Beckwith-Wiedemann Syndrome According to Genotype/Epigenotype Subgroups

Fetal and pediatric pathology, 2018-11, Vol.37 (6), p.387-399

2018

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Beckwith-Wiedemann syndrome with overlapping Perlman syndrome manifestation

The journal of maternal-fetal & neonatal medicine, 2014-10, Vol.27 (15), p.1607-1609

2014

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The placenta in Beckwith-Wiedemann syndrome: genotype-phenotype associations, excessive extravillous trophoblast and placental mesenchymal dysplasia

Pathology, 2012-10, Vol.44 (6), p.519-527

2012

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

Fetal and pediatric pathology, 2018-11, Vol.37 (6), p.411-417

2018

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Derivation and investigation of the first human cell-based model of Beckwith-Wiedemann syndrome

Epigenetics, 2021-12, Vol.16 (12), p.1295-1305

2021

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Use of multilocus methylation-specific single nucleotide primer extension (MS-SNuPE) technology in diagnostic testing for human imprinted loci

Epigenetics, 2012-05, Vol.7 (5), p.473-481

2012

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Localized Placental Mesenchymal Dysplasia in Monochorionic Diamniotic Twin Placenta with Beckwith-Wiedemann Syndrome

Fetal and pediatric pathology, 2022-07, Vol.41 (4), p.1-664

2022

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Novel Autopsy Findings in Premature Infant With Beckwith-Wiedemann Syndrome Uniparental Disomy: Multifocal Developmental Dysplastic Chrondromatous Lesions and Cortical Neuronal Heterotopias

Fetal and pediatric pathology, 2024-04, p.1-9

2024

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Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

Epigenetics, 2013-10, Vol.8 (10), p.1053-1060

2013

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Macroglossia and speech in Beckwith-Wiedemann syndrome: a sample survey study

International journal of language & communication disorders, 1999-04, Vol.34 (2), p.209-221

1999

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Angiogenesis-related biomarkers (sFlt-1/PlGF) in placental mesenchymal dysplasia

The journal of maternal-fetal & neonatal medicine, 2017-04, Vol.30 (8), p.958-961

2017

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Molecular Pathogenesis of Rhabdomyosarcoma

Cancer biology & therapy, 2002-03, Vol.1 (2), p.97-104

2002

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Lessons from imprinted multilocus loss of methylation in human syndromes: A step toward understanding the mechanisms underlying these complex diseases

Epigenetics, 2010-07, Vol.5 (5), p.373-377

2010

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"DOUBLE-MUSCLE" TRAIT IN CATTLE: A POSSIBLE MODEL FOR WIEDEMANN-BECKWITH SYNDROME

Fetal and pediatric pathology, 2006-01, Vol.25 (1), p.9-20

2006

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Bone Invasion by a Recurrent Digital Fibroma of Infancy in a Child with Beckwith-Wiedemann Syndrome

Fetal and pediatric pathology, 1995, Vol.15 (1), p.147-151

1995

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Spontaneous and ART-induced large offspring syndrome: similarities and differences in DNA methylome

Epigenetics, 2022-11, Vol.17 (11), p.1477-1496

2022

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VASCULAR MALFORMATION AND CHOROID PLEXUS ADRENAL HETEROTOPIA: NEW FINDINGS IN BECKWITH-WIEDEMANN SYNDROME?

Fetal and pediatric pathology, 2006-07, Vol.25 (4), p.191-197

2006

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Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders

Epigenetics, 2018-09, Vol.13 (9), p.897-909

2018

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Small regulatory RNAs controlled by genomic imprinting and their contribution to human disease

Epigenetics, 2012-12, Vol.7 (12), p.1341-1348

2012

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Speech and oral motor skills in children with Beckwith Wiedemann Syndrome: Pre- and post-tongue reduction surgery

Advances in speech-language pathology, 2006-03, Vol.8 (1), p.45-55

2006

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Beckwith-Wiedemann Syndrome: Prenatal Ultrasonic Diagnosis and Clinical Implications

The Journal of maternal-fetal medicine, 1992-01, Vol.1 (2), p.70-74

1992

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

Altered microRNA expression profiles in large offspring syndrome and Beckwith-Wiedemann syndrome

Beckwith-Wiedemann Syndrome, Delayed Abdominal Wall Closure, and Neonatal Intussusception -Case Report and Literature Review

Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi

Placental Pathology in Beckwith-Wiedemann Syndrome According to Genotype/Epigenotype Subgroups

Beckwith-Wiedemann syndrome with overlapping Perlman syndrome manifestation

The placenta in Beckwith-Wiedemann syndrome: genotype-phenotype associations, excessive extravillous trophoblast and placental mesenchymal dysplasia

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

Derivation and investigation of the first human cell-based model of Beckwith-Wiedemann syndrome

Use of multilocus methylation-specific single nucleotide primer extension (MS-SNuPE) technology in diagnostic testing for human imprinted loci

Localized Placental Mesenchymal Dysplasia in Monochorionic Diamniotic Twin Placenta with Beckwith-Wiedemann Syndrome

Novel Autopsy Findings in Premature Infant With Beckwith-Wiedemann Syndrome Uniparental Disomy: Multifocal Developmental Dysplastic Chrondromatous Lesions and Cortical Neuronal Heterotopias

Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

Macroglossia and speech in Beckwith-Wiedemann syndrome: a sample survey study

Angiogenesis-related biomarkers (sFlt-1/PlGF) in placental mesenchymal dysplasia

Molecular Pathogenesis of Rhabdomyosarcoma

Lessons from imprinted multilocus loss of methylation in human syndromes: A step toward understanding the mechanisms underlying these complex diseases

"DOUBLE-MUSCLE" TRAIT IN CATTLE: A POSSIBLE MODEL FOR WIEDEMANN-BECKWITH SYNDROME

Bone Invasion by a Recurrent Digital Fibroma of Infancy in a Child with Beckwith-Wiedemann Syndrome

Spontaneous and ART-induced large offspring syndrome: similarities and differences in DNA methylome

VASCULAR MALFORMATION AND CHOROID PLEXUS ADRENAL HETEROTOPIA: NEW FINDINGS IN BECKWITH-WIEDEMANN SYNDROME?

Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders

Small regulatory RNAs controlled by genomic imprinting and their contribution to human disease

Speech and oral motor skills in children with Beckwith Wiedemann Syndrome: Pre- and post-tongue reduction surgery

Beckwith-Wiedemann Syndrome: Prenatal Ultrasonic Diagnosis and Clinical Implications

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