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A founder variant expands the phenotype of WNT7B ‐related PDAC syndrome
A founder variant expands the phenotype of WNT7B ‐related PDAC syndrome
Fuente:
Wiley Open Access
Saved in:
Bibliographic Details
Main Authors:
Lama AlAbdi
,
Zuhair Rahbeeni
,
Sateesh Maddirevula
,
Rana Helaby
,
Firdous Abdulwahab
,
Arif O. Khan
,
Lisa G. Riley
,
Amal Alhashem
,
Nicolas Chassaing
,
Robyn V. Jamieson
,
Fowzan S. Alkuraya
Format:
Artículo Open Access
Published:
Wiley
2024
Subjects:
Clinical Genetics
Online Access:
Acceder al recurso
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https://onlinelibrary.wiley.com/doi/10.1111/cge.14512
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