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Beckwith-wiedemann spectrum
Eamonn R. Maher
*
*
Corresponding author for this work
Aston Medical School
College of Health and Life Sciences
Research output
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Chapter in Book/Published conference output
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Keyphrases
Beckwith-Wiedemann Syndrome
100%
Lateralized Overgrowth
50%
Imprinted Genes
33%
Molecular Abnormalities
33%
Embryonal Tumor
33%
Chromosome 11p15
33%
Exomphalos
33%
Gene Cluster
16%
Clinical Features
16%
Genotype-phenotype Correlation
16%
Aberrant Expression
16%
Phenotypic Variation
16%
Overgrowth
16%
Molecular Aspects
16%
International Consensus
16%
Consensus Statement
16%
Clinical Aspects
16%
Wilms Tumor
16%
Anterior Abdominal Wall Defect
16%
Imprinting Disorders
16%
Epigenotype
16%
Epimutation
16%
Tumor Risk
16%
Hemihypertrophy
16%
Molecular Subgroups
16%
Neonatal Hypoglycemia
16%
Macroglossia
16%
Imprinting Center
16%
Biochemistry, Genetics and Molecular Biology
Gene Cluster
100%
Autosome
100%
Epimutation
100%
Wilms' Tumor
100%
Medicine and Dentistry
Beckwith Wiedemann Syndrome
100%
Umbilical Hernia
33%
Neoplasm
16%
Clinical Feature
16%
Disease Predisposition
16%
Wilms' Tumor
16%
Abdominal Wall Defect
16%
Hemihypertrophy
16%
Neonatal Hypoglycemia
16%
Macroglossia
16%
Autosome
16%
Gene Cluster
16%
Diseases
16%
Tumor
16%