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
Novel NOG (p.P42S) mutation causes proximal symphalangism in a four-generation Chinese family.
Sha Y et al.
Bmc Medical Genetics, 2019
Multiple synostoses syndrome in three members of a family displaying a novel mutation in NOGGIN gene.
Aydin HU et al.
Journal of Plastic, Reconstructive & Aesthetic Surgery : Jpras, 2013
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