Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference21 articles.
1. Morisada N, Nozu K, Iijima K. Branchio-oto-renal syndrome: comprehensive review based on nationwide surveillance in Japan. Pediatr Int. 2014;56:309–14.
2. Smith RJH. In: Branchiootorenal spectrum disorders. Pagon RA, Adam MP, Ardinger HH, (eds). GeneReviews. Seattle: University of Washington; 2015.
3. Fraser FC, Sproule JR, Halal F, Optiz JM. Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss. Am J Med Genet A. 1980;7:341–9.
4. Engels S, Kohlhase J, McGaughran J. ASALL1 mutation causes a branchio-oto-renal syndrome-like phenotype. J Med Genet. 2000;37:458–60.
5. Morisada N, Sekine T, Ishimori S, Tsuda M, Adachi M, Nozu K, et al. 16q12 microdeletion syndrome in two Japanese boys. Pediatr Int. 2014;56:e75–8.
Cited by
35 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献