Associated Papers
Molecular underpinnings of exceptional response in primary malignant melanoma of the esophagus to anti-PD-1 monotherapy.
Dai J et al.
Journal for Immunotherapy of Cancer, 2023
36593066 (PubMed )
Supplement: jitc-2022-005937supp007.xls › Supplemental_Table_3
Multi-layered mutation in hedgehog-related genes in Gorlin syndrome may affect the phenotype.
Onodera S et al.
Plos One, 2017
Mutations in WNT9B are associated with Mayer-Rokitansky-Küster-Hauser syndrome.
Waschk DE et al.
Clinical Genetics, 2016
WNT9B in 542 Chinese women with Müllerian duct abnormalities: mutation analysis.
Tang R et al.
Reproductive Biomedicine Online, 2014
Novel compound heterozygous mutations of ALDH1A3 contribute to anophthalmia in a non-consanguineous Chinese family.
Liu Y et al.
Genetics and Molecular Biology, 0
28590501 (PubMed )
Supplement: 1415-4757-gmb-1678-4685-GMB-2016-0120-Suppl03.pdf
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