Associated Papers
Clinical observation and genetic analysis of a SYNS1 family caused by novel NOG gene mutation.
Zhang Z et al.
Molecular Genetics & Genomic Medicine, 2022
Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling.
Ma C et al.
Bmc Medical Genetics, 2019
Identification of two novel mutations in the NOG gene associated with congenital stapes ankylosis and symphalangism.
Ganaha A et al.
Journal of Human Genetics, 2015
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