SECOND CASE OF HEPATOBLASTOMA IN A YOUNG PATIENT WITH SIMPSON-GOLABI-BEHMEL SYNDROME
Author:
Publisher
Informa UK Limited
Subject
Oncology,Hematology,Pediatrics, Perinatology and Child Health
Link
http://www.tandfonline.com/doi/pdf/10.1080/08880010500198988
Reference9 articles.
1. Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
2. Genotype/Phenotype Correlations of Males Affected by Simpson-Golabi-Behmel Syndrome with GPC3 Gene Mutations: Patient Report and Review of the Literature
3. Developmental changes in heparan sulfate expression: in situ detection with mAbs.
4. GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome
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1. Phenotypic spectrum and tumor risk in Simpson‐Golabi‐Behmel syndrome: Case series and comprehensive literature review;American Journal of Medical Genetics Part A;2024-08-19
2. Hepatoblastoma in molecularly defined, congenital diseases;American Journal of Medical Genetics Part A;2022-04-28
3. Simpson-Golabi-Behmel syndrome;Radiopaedia.org;2020-11-24
4. Acute lymphoblastic leukemia in a male with Simpson–Golabi–Behmel syndrome;American Journal of Medical Genetics Part A;2018-05-07
5. Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma;Clinical Cancer Research;2017-07-01
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