[PDF][PDF] Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith‐Wiedemann syndrome

NS Sobel Naveh, EM Traxler, KA Duffy… - Hepatology …, 2022 - Wiley Online Library
Abstract Beckwith‐Wiedemann Syndrome (BWS) is the most common human overgrowth
disorder caused by structural and epigenetic changes to chromosome 11p15. Patients with …

Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith-Wiedemann syndrome.

SN NS, EM Traxler, KA Duffy… - Hepatology …, 2022 - europepmc.org
Abstract Beckwith‐Wiedemann Syndrome (BWS) is the most common human overgrowth
disorder caused by structural and epigenetic changes to chromosome 11p15. Patients with …

[HTML][HTML] Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith‐Wiedemann syndrome

NSS Naveh, EM Traxler, KA Duffy… - Hepatology …, 2022 - ncbi.nlm.nih.gov
Abstract Beckwith‐Wiedemann Syndrome (BWS) is the most common human overgrowth
disorder caused by structural and epigenetic changes to chromosome 11p15. Patients with …

Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith-Wiedemann syndrome

NSS Naveh, EM Traxler, KA Duffy… - Hepatology …, 2022 - pubmed.ncbi.nlm.nih.gov
Beckwith-Wiedemann Syndrome (BWS) is the most common human overgrowth disorder
caused by structural and epigenetic changes to chromosome 11p15. Patients with BWS are …

[HTML][HTML] Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith‐Wiedemann syndrome

NSS Naveh, EM Traxler, KA Duffy… - Hepatology …, 2022 - journals.lww.com
Abstract Beckwith‐Wiedemann Syndrome (BWS) is the most common human overgrowth
disorder caused by structural and epigenetic changes to chromosome 11p15. Patients with …

Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith‐Wiedemann syndrome

NSS Naveh, EM Traxler, KA Duffy… - Hepatology …, 2022 - search.proquest.com
Abstract Beckwith‐Wiedemann Syndrome (BWS) is the most common human overgrowth
disorder caused by structural and epigenetic changes to chromosome 11p15. Patients with …