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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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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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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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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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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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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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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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Assisted reproductive therapies and imprinting disorders—a preliminary British survey

Human reproduction (Oxford), 2006-04, Vol.21 (4), p.1009-1011

2006

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Imprinting Mutation in the Beckwith-Wiedemann Syndrome Leads to Biallelic IGF2 expression through an H19-Independent Pathway

Human molecular genetics, 1996-12, Vol.5 (12), p.2027-2032

1996

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A survey of assisted reproductive technology births and imprinting disorders

Human reproduction (Oxford), 2007-12, Vol.22 (12), p.3237-3240

2007

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Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith—Wiedemann syndrome

Human molecular genetics, 1995-03, Vol.4 (3), p.395-399

1995

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Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse

Human molecular genetics, 2000-07, Vol.9 (12), p.1829-1841

2000

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Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome

Human molecular genetics, 2000-09, Vol.9 (14), p.2075-2083

2000

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Syntenic Organization of the Mouse Distal Chromosome 7 Imprinting Cluster and the Beckwith-Wiedemann Syndrome Region in Chromosome 11p15.5

Human molecular genetics, 1998-07, Vol.7 (7), p.1149-1159

1998

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Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression

Human molecular genetics, 2000-01, Vol.9 (2), p.203-216

2000

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Beckwith-Wiedemann syndrome and Wilms' tumour

Molecular human reproduction, 1997-02, Vol.3 (2), p.157-168

WARD, A

1997

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Infertility, assisted reproduction technologies and imprinting disturbances: a Dutch study

Human reproduction (Oxford), 2007-09, Vol.22 (9), p.2476-2480

2007

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Epigenetic risks related to assisted reproductive technologies: Epigenetics, imprinting, ART and icebergs?

Human reproduction (Oxford), 2003-12, Vol.18 (12), p.2508-2511

2003

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Parental infertility, infertility treatment and hepatoblastoma: a report from the Children's Oncology Group

Human reproduction (Oxford), 2012-06, Vol.27 (6), p.1649-1656

2012

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Hyperinsulinism in Infancy and Childhood: When an Insulin Level Is Not Always Enough

Clinical chemistry (Baltimore, Md.), 2008-02, Vol.54 (2), p.256-263

2008

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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

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

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

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

Allelic methylation of H19 and IGF2 in the 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

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

Assisted reproductive therapies and imprinting disorders—a preliminary British survey

Imprinting Mutation in the Beckwith-Wiedemann Syndrome Leads to Biallelic IGF2 expression through an H19-Independent Pathway

A survey of assisted reproductive technology births and imprinting disorders

Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith—Wiedemann syndrome

Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse

Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome

Syntenic Organization of the Mouse Distal Chromosome 7 Imprinting Cluster and the Beckwith-Wiedemann Syndrome Region in Chromosome 11p15.5

Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression

Beckwith-Wiedemann syndrome and Wilms' tumour

Infertility, assisted reproduction technologies and imprinting disturbances: a Dutch study

Epigenetic risks related to assisted reproductive technologies: Epigenetics, imprinting, ART and icebergs?

Parental infertility, infertility treatment and hepatoblastoma: a report from the Children's Oncology Group

Hyperinsulinism in Infancy and Childhood: When an Insulin Level Is Not Always Enough

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