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
A novel DLL4 missense mutation in a Chinese patient with Adams-Oliver syndrome.
Yu X et al.
Chinese Medical Journal, 2019
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
[Identification of a new missense mutation in a Chinese family with inherited long QT syndrome (no abstract)].
Yang HT et al.
Zhonghua Xin Xue Guan Bing Za Zhi, 2008
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