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Chen CP, Ko TM, Chang TY, Chern SR, Chen SW, Lai ST, Chuang TY, Wang W. Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus. Taiwan J Obstet Gynecol. 2018; 57:123-127.","DOI":"10.1016\/j.tjog.2017.12.021"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. McInerney-Leo AM, Harris JE, Leo PJ, <i>et al.<\/i> Whole exome sequencing is an efficient, sensitive and specific method for determining the genetic cause of short-rib thoracic dystrophies. Clin Genet. 2015; 88:550-557.","DOI":"10.1111\/cge.12550"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Dagoneau N, Goulet M, Genevi\u00e8ve D, <i>et al.<\/i> DYNC2H1 mutations cause asphyxiating thoracic dystrophy and short rib-polydactyly syndrome, type III. 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Targeted next generation sequencing identifies novel compound heterozygous mutations of DYNC2H1 in a fetus with short rib-polydactyly syndrome, type III. Clin Chim Acta. 2015; 447:47-51.","DOI":"10.1016\/j.cca.2015.05.005"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Yi P, Li WJ, Dong MQ, Ou G. Dynein-driven retrograde intraflagellar transport is triphasic in C. elegans sensory cilia. Curr Biol. 2017; 27:1448-1461.","DOI":"10.1016\/j.cub.2017.04.015"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Zhang W, Taylor SP, Ennis HA, <i>et al.<\/i> Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathies. Hum Mutat. 2018; 39:152-166.","DOI":"10.1002\/humu.23362"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Merrill AE, Merriman B, Farrington-Rock C, <i>et al.<\/i> Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome. 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