Associated Papers
A novel DLL4 mutation in Adams-Oliver syndrome with absence of the right pulmonary artery in newborn.
Rojnueangnit K et al.
American Journal of Medical Genetics. Part A, 2022
ConVarT: a search engine for matching human genetic variants with variants from non-human species.
Pir MS et al.
Nucleic Acids Research, 2022
34718716 (PubMed )
Supplement: gkab939_supplemental_files.zip › Table_S13.xls › human_pat_mouse_phe_orthovar_14
Elucidating the genetic architecture of Adams-Oliver syndrome in a large European cohort.
Meester JAN et al.
Human Mutation, 2018
Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.
Nagasaka M et al.
Journal of Human Genetics, 2017
The developmental biology of genetic Notch disorders.
Mašek J et al.
Development (cambridge, England), 2017
28512196 (PubMed )
Supplement: supplement_1.pdf
EOGT and O-GlcNAc on secreted and membrane proteins.
Varshney S et al.
Biochemical Society Transactions, 2017
Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome.
Meester JA et al.
American Journal of Human Genetics, 2015
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