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
Multiple synostoses syndrome: Clinical report and retrospective analysis.
Pan Z et al.
American Journal of Medical Genetics. Part A, 2020
Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling.
Ma C et al.
Bmc Medical Genetics, 2019
A novel nonsense mutation in the NOG gene causes familial NOG-related symphalangism spectrum disorder.
Takano K et al.
Human Genome Variation, 2016
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
Missing Links Between Genetically Inherited Molecules in Split Cord Malformation and Other Anomaly: A Bench to Bedside Approach.
Barik M et al.
Journal of Pediatric Neurosciences, 0
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