Sharova, M.; Markova, T.; Sumina, M.; Petukhova, M.; Bulakh, M.; Ryzhkova, O.; Nagornova, T.; Ionova, S.; Marakhonov, A.; Dadali, E.;
et al. Rare IFT140-Associated Phenotype of Cranioectodermal Dysplasia and Features of Diagnostic Journey in Patients with Suspected Ciliopathies. Genes 2023, 14, 1553.
https://doi.org/10.3390/genes14081553
AMA Style
Sharova M, Markova T, Sumina M, Petukhova M, Bulakh M, Ryzhkova O, Nagornova T, Ionova S, Marakhonov A, Dadali E,
et al. Rare IFT140-Associated Phenotype of Cranioectodermal Dysplasia and Features of Diagnostic Journey in Patients with Suspected Ciliopathies. Genes. 2023; 14(8):1553.
https://doi.org/10.3390/genes14081553
Chicago/Turabian Style
Sharova, Margarita, Tatyana Markova, Maria Sumina, Marina Petukhova, Maria Bulakh, Oxana Ryzhkova, Tatyana Nagornova, Sofya Ionova, Andrey Marakhonov, Elena Dadali,
and et al. 2023. "Rare IFT140-Associated Phenotype of Cranioectodermal Dysplasia and Features of Diagnostic Journey in Patients with Suspected Ciliopathies" Genes 14, no. 8: 1553.
https://doi.org/10.3390/genes14081553
APA Style
Sharova, M., Markova, T., Sumina, M., Petukhova, M., Bulakh, M., Ryzhkova, O., Nagornova, T., Ionova, S., Marakhonov, A., Dadali, E., & Kutsev, S.
(2023). Rare IFT140-Associated Phenotype of Cranioectodermal Dysplasia and Features of Diagnostic Journey in Patients with Suspected Ciliopathies. Genes, 14(8), 1553.
https://doi.org/10.3390/genes14081553