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Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome

European journal of human genetics : EJHG, 2005-09, Vol.13 (9), p.1025-1032

2005

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A Maternally Methylated CpG Island in KvLQT1 Is Associated with an Antisense Paternal Transcript and Loss of Imprinting in Beckwith-Wiedemann Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1999-07, Vol.96 (14), p.8064-8069

1999

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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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Frequent RASSF1A tumour suppressor gene promoter methylation in Wilms' tumour and colorectal cancer

Oncogene, 2002-10, Vol.21 (47), p.7277-7282

2002

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novH: differential expression in developing kidney and Wilm's tumors

The American journal of pathology, 1998-06, Vol.152 (6), p.1563-1575

1998

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Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation

Journal of medical genetics, 1999-07, Vol.36 (7), p.518-523

1999

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PRIME importance of pathology expertise

Nature biotechnology, 2009-01, Vol.27 (1), p.24-25

2009

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impending crisis in the provision of histopathology expertise for mouse functional genomics

The Journal of pathology, 2009, Vol.217 (1), p.4-13

2009

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Pathbase: a database of mutant mouse pathology

Nucleic acids research, 2004-01, Vol.32 (Database issue), p.D512-515

2004

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Altered expression of novH is associated with human adrenocortical tumorigenesis

The journal of clinical endocrinology and metabolism, 2001-08, Vol.86 (8), p.3929-3940

2001

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Progress in updating the European Radiobiology Archives

International journal of radiation biology, 2008-01, Vol.84 (11), p.930-936

2008

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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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Expression of the human NOV gene in first trimester fetal tissues

Anatomy and Embryology, 2001-06, Vol.203 (6), p.417-427

2001

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Expression of the Von Hippel—Lindau Disease Tumour Suppressor Gene during Human Embryogenesis

Human molecular genetics, 1996-05, Vol.5 (5), p.639-644

1996

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Genomic imprinting and cancer; new paradigms in the genetics of neoplasia

Toxicology letters, 2001-03, Vol.120 (1), p.151-160

2001

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Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome

Journal of medical genetics, 1997-05, Vol.34 (5), p.353-359

1997

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Mouse Nov gene is expressed in hypaxial musculature and cranial structures derived from neural crest cells and placodes

Developmental dynamics, 2000-11, Vol.219 (3), p.417-425

2000

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Growth factors, cytokines and soluble forms of receptor molecules in cancer patients

Anticancer research, 1995-03, Vol.15 (2), p.343

1995

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Impact of genomic imprinting on genomic instability and radiation-induced mutation

International journal of radiation biology, 1998, Vol.74 (6), p.705-710

SCHOFIELD, P. N.

1998

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Mosaic uniparental disomy in Beckwith-Wiedemann syndrome

Journal of medical genetics, 1994-10, Vol.31 (10), p.749-753

1994

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Pathbase: a new reference resource and database for laboratory mouse pathology

Radiation protection dosimetry, 2004-01, Vol.112 (4), p.525-528

2004

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Effects of insulin and insulin-like growth factors I and II on the growth of equine fetal and neonatal chondrocytes

Equine veterinary journal, 1997-11, Vol.29 (6), p.441-447

1997

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Molecular and Functional Characterization of Amylin, a Peptide Associated with Type 2 Diabetes Mellitus

Proceedings of the National Academy of Sciences - PNAS, 1989-12, Vol.86 (24), p.9662-9666

1989

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Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome

Journal of medical genetics, 2000-03, Vol.37 (3), p.212-215

2000

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Temporal changes in the expression of the insulin-like growth factor II gene associated with tissue maturation in the human fetus

Development (Cambridge), 1989-07, Vol.106 (3), p.543-554

1989

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Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome

A Maternally Methylated CpG Island in KvLQT1 Is Associated with an Antisense Paternal Transcript and Loss of Imprinting in Beckwith-Wiedemann Syndrome

Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

Frequent RASSF1A tumour suppressor gene promoter methylation in Wilms' tumour and colorectal cancer

novH: differential expression in developing kidney and Wilm's tumors

Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation

PRIME importance of pathology expertise

impending crisis in the provision of histopathology expertise for mouse functional genomics

Pathbase: a database of mutant mouse pathology

Altered expression of novH is associated with human adrenocortical tumorigenesis

Progress in updating the European Radiobiology Archives

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

Expression of the human NOV gene in first trimester fetal tissues

Expression of the Von Hippel—Lindau Disease Tumour Suppressor Gene during Human Embryogenesis

Genomic imprinting and cancer; new paradigms in the genetics of neoplasia

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome

Mouse Nov gene is expressed in hypaxial musculature and cranial structures derived from neural crest cells and placodes

Growth factors, cytokines and soluble forms of receptor molecules in cancer patients

Impact of genomic imprinting on genomic instability and radiation-induced mutation

Mosaic uniparental disomy in Beckwith-Wiedemann syndrome

Pathbase: a new reference resource and database for laboratory mouse pathology

Effects of insulin and insulin-like growth factors I and II on the growth of equine fetal and neonatal chondrocytes

Molecular and Functional Characterization of Amylin, a Peptide Associated with Type 2 Diabetes Mellitus

Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome

Temporal changes in the expression of the insulin-like growth factor II gene associated with tissue maturation in the human fetus

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