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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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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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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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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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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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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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Paradoxical NSD1 Mutations in Beckwith-Wiedemann Syndrome and 11p15 Anomalies in Sotos Syndrome

American journal of human genetics, 2004-04, Vol.74 (4), p.715-720

2004

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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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Serum α-fetoprotein screening for hepatoblastoma in children with Beckwith-Wiedemann syndrome or isolated hemihyperplasia

The Journal of pediatrics, 2003-08, Vol.143 (2), p.270-272

2003

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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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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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Imprinting Status of 11p15 Genes in Beckwith–Wiedemann Syndrome Patients with CDKN1C Mutations

Genomics (San Diego, Calif.), 2001-06, Vol.74 (3), p.370-376

2001

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Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation : Occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS

Human molecular genetics, 2001-03, Vol.10 (5), p.467-476

2001

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Hypercalciuria in Beckwith-Wiedemann syndrome

The Journal of pediatrics, 2003-02, Vol.142 (2), p.206-208

2003

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Beckwith-Wiedemann Syndrome: An Update and Review for the Primary Pediatrician

Clinical pediatrics, 1995-06, Vol.34 (6), p.317-326

1995

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Genetic linkage of Beckwith-Wiedemann syndrome to 11p15

American journal of human genetics, 1989-05, Vol.44 (5), p.720-723

1989

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Ectopic spleen and left-sided vena cava in Beckwith–Wiedemann syndrome

Computerized medical imaging and graphics, 2002-05, Vol.26 (3), p.177-180

2002

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Taste after reduction of the tongue in Beckwith–Wiedemann syndrome

British journal of oral & maxillofacial surgery, 2006-02, Vol.44 (1), p.49-51

2006

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Nonmalignant renal disease in pediatric patients with Beckwith-Wiedemann syndrome

American journal of roentgenology (1976), 1998-09, Vol.171 (3), p.733

1998

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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

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

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

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

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

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

Paradoxical NSD1 Mutations in Beckwith-Wiedemann Syndrome and 11p15 Anomalies in Sotos 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

Serum α-fetoprotein screening for hepatoblastoma in children with Beckwith-Wiedemann syndrome or isolated hemihyperplasia

Hyperinsulinism and Beckwith-Wiedemann syndrome

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

Imprinting Status of 11p15 Genes in Beckwith–Wiedemann Syndrome Patients with CDKN1C Mutations

Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation : Occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS

Hypercalciuria in Beckwith-Wiedemann syndrome

Beckwith-Wiedemann Syndrome: An Update and Review for the Primary Pediatrician

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15

Ectopic spleen and left-sided vena cava in Beckwith–Wiedemann syndrome

Taste after reduction of the tongue in Beckwith–Wiedemann syndrome

Nonmalignant renal disease in pediatric patients with Beckwith-Wiedemann syndrome

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