Associated Papers
Whole-exome sequencing reveals causative genetic variants for several overgrowth syndromes in molecularly negative Beckwith-Wiedemann spectrum.
Higashimoto K et al.
Journal of Medical Genetics, 2024
Mutation update for the GPC3 gene involved in Simpson-Golabi-Behmel syndrome and review of the literature.
Vuillaume ML et al.
Human Mutation, 2018
Mutation update for the GPC3 gene involved in Simpson-Golabi-Behmel syndrome and review of the literature.
Vuillaume ML et al.
Human Mutation, 2018
GPC3 mutations in seven patients with Simpson-Golabi-Behmel syndrome.
Sakazume S et al.
American Journal of Medical Genetics. Part A, 2007
Novel nonsense mutation of GPC3 gene in a patient with Simpson-Golabi-Behmel syndrome.
Ratbi I et al.
The Turkish Journal of Pediatrics, 0
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