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Hepatic Malignancy in an Infant with Wolf–Hirschhorn Syndrome
Sara Rutter
, Raffaella A. Morotti
, Steven Peterec
, Patrick G. Gallagher
Research output
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peer-review
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Keyphrases
Growth Failure
100%
Hepatic Malignancy
100%
Seizure
50%
Liver
50%
Hepatocellular Carcinoma
50%
Autopsy
50%
Genetic Studies
50%
Immunohistochemical Staining
50%
Histologic Examination
50%
Nodule
50%
Ki-67
50%
Hepatoblastoma
50%
Cardiac Defects
50%
Terminal Deletion
50%
Glypican-3 (GPC3)
50%
CD34 Expression
50%
Sinusoidal Endothelial Cells
50%
Cell Plate
50%
Glutamine Synthetase
50%
Craniofacial Features
50%
Nodular Lesion
50%
Complex Congenital Heart Disease
50%
Contiguous Gene Syndrome
50%
Failure Characteristics
50%
Cytological Atypia
50%
Chromosome 4p
50%
Medicine and Dentistry
Cancer
100%
Growth Disorder
100%
Epileptic Seizure
50%
Hepatocellular Carcinoma
50%
Glypican 3
50%
Glutamate Ammonia Ligase
50%
Craniofacial Malformation
50%
Hepatoblastoma
50%
Complex Congenital Heart Disease
50%
Chromosome 4p
50%
Cell Plate
50%
Genetics
50%
Chromosome
50%
Endothelium
50%