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The epigenetic imprinting defect of patients with Beckwith—Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region

Journal of medical genetics, 2006-12, Vol.43 (12), p.902-907

2006

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Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith–Wiedemann syndrome and Wilms' tumour

Human molecular genetics, 2008-05, Vol.17 (10), p.1427-1435

2008

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Clinical and molecular genetic features of Beckwith–Wiedemann syndrome associated with assisted reproductive technologies

Human reproduction (Oxford), 2009-03, Vol.24 (3), p.741-747

2009

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Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome

European journal of human genetics : EJHG, 2009-05, Vol.17 (5), p.611-619

2009

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Beckwith-Wiedemann Syndrome and Juvenile Fibroadenoma: A Case Report

Annals of plastic surgery, 2010-06, Vol.64 (6), p.803-806

2010

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Beckwith-Wiedemann syndrome in a child with Chiari I malformation. Case report

Journal of neurosurgery, 2005-08, Vol.103 (2 Suppl), p.172

2005

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Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith–Wiedemann syndrome

Human molecular genetics, 2002-05, Vol.11 (11), p.1317-1325

2002

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Mechanisms causing imprinting defects in familial Beckwith–Wiedemann syndrome with Wilms' tumour

Human molecular genetics, 2007-02, Vol.16 (3), p.254-264

2007

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Imprinting mutations in the Beckwith—Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2–H19 domain

Human molecular genetics, 1995-12, Vol.4 (12), p.2379-2385

1995

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A review of known imprinting syndromes and their association with assisted reproduction technologies

Human reproduction (Oxford), 2008-12, Vol.23 (12), p.2826-2834

2008

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Characterization of DNA methylation errors in patients with imprinting disorders conceived by assisted reproduction technologies

Human reproduction (Oxford), 2012-08, Vol.27 (8), p.2541-2548

2012

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Neonatal hepatoblastoma in a newborn with severe phenotype of Beckwith–Wiedemann syndrome

European journal of pediatrics, 2011-11, Vol.170 (11), p.1407-1411

2011

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Imprinting of IGF2 and H19: Lack of Reciprocity in Sporadic Beckwith-Wiedemann Syndrome

Human molecular genetics, 1997-09, Vol.6 (9), p.1543-1548

1997

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Double Stellate Tongue Reduction: A New Method of Treatment for Macroglossia in Patients With Beckwith-Wiedemann Syndrome

Annals of plastic surgery, 2011-09, Vol.67 (3), p.240-244

2011

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Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome

Nature (London), 1997-10, Vol.389 (6653), p.809-815

1997

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Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

Journal of medical genetics, 2000-12, Vol.37 (12), p.921-926

2000

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No evidence for pathogenic variants or maternal effect of ZFP57 as the cause of Beckwith-Wiedemann Syndrome

European journal of human genetics : EJHG, 2012-01, Vol.20 (1), p.119-121

2012

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Hyperinsulinemic Hypoglycemia in Beckwith-Wiedemann Syndrome due to Defects in the Function of Pancreatic β-Cell Adenosine Triphosphate-Sensitive Potassium Channels

The journal of clinical endocrinology and metabolism, 2005-07, Vol.90 (7), p.4376-4382

2005

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Epimutation of the TNDM locus and the Beckwith-Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitus

Human genetics, 2006-03, Vol.119 (1-2), p.179-184

2006

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Allelic methylation of H19 and IGF2 in the Beckwith — Wiedemann syndrome

Human molecular genetics, 1994-08, Vol.3 (8), p.1297-1301

1994

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Hyperinsulinism and Beckwith-Wiedemann syndrome

Archives of disease in childhood. Fetal and neonatal edition, 2001-01, Vol.84 (1), p.F67

2001

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Placental mesenchymal dysplasia is associated with high rates of intrauterine growth restriction and fetal demise : A report of 11 new cases and a review of the literature

American journal of clinical pathology, 2006-07, Vol.126 (1), p.67-78

2006

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The 5' end of the KCNQ10T1 gene is hypomethylated in the Beckwith-Wiedemann syndrome

Human genetics, 2002-07, Vol.111 (1), p.105-107

2002

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Alternative mechanisms associated with silencing of CDKN1C in Beckwith–Wiedemann syndrome

Journal of medical genetics, 2005-08, Vol.42 (8), p.648-655

2005

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Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome

Nature genetics, 2012-07, Vol.44 (7), p.788-792

2012

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The epigenetic imprinting defect of patients with Beckwith—Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region

Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith–Wiedemann syndrome and Wilms' tumour

Clinical and molecular genetic features of Beckwith–Wiedemann syndrome associated with assisted reproductive technologies

Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome

Beckwith-Wiedemann Syndrome and Juvenile Fibroadenoma: A Case Report

Beckwith-Wiedemann syndrome in a child with Chiari I malformation. Case report

Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith–Wiedemann syndrome

Mechanisms causing imprinting defects in familial Beckwith–Wiedemann syndrome with Wilms' tumour

Imprinting mutations in the Beckwith—Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2–H19 domain

A review of known imprinting syndromes and their association with assisted reproduction technologies

Characterization of DNA methylation errors in patients with imprinting disorders conceived by assisted reproduction technologies

Neonatal hepatoblastoma in a newborn with severe phenotype of Beckwith–Wiedemann syndrome

Imprinting of IGF2 and H19: Lack of Reciprocity in Sporadic Beckwith-Wiedemann Syndrome

Double Stellate Tongue Reduction: A New Method of Treatment for Macroglossia in Patients With Beckwith-Wiedemann Syndrome

Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome

Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

No evidence for pathogenic variants or maternal effect of ZFP57 as the cause of Beckwith-Wiedemann Syndrome

Hyperinsulinemic Hypoglycemia in Beckwith-Wiedemann Syndrome due to Defects in the Function of Pancreatic β-Cell Adenosine Triphosphate-Sensitive Potassium Channels

Epimutation of the TNDM locus and the Beckwith-Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitus

Allelic methylation of H19 and IGF2 in the Beckwith — Wiedemann syndrome

Hyperinsulinism and Beckwith-Wiedemann syndrome

Placental mesenchymal dysplasia is associated with high rates of intrauterine growth restriction and fetal demise : A report of 11 new cases and a review of the literature

The 5' end of the KCNQ10T1 gene is hypomethylated in the Beckwith-Wiedemann syndrome

Alternative mechanisms associated with silencing of CDKN1C in Beckwith–Wiedemann syndrome

Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome

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