Author:
Valikodath Nita G.,Jain Samiksha,Miller Marilyn,Kaufman Lawrence M.
Subject
Ophthalmology,Pediatrics, Perinatology, and Child Health
Reference9 articles.
1. Townes-Brocks Syndrome;Kohlhase,1993
2. Atypical phenotype and intrafamilial variability associated with a novel SALL1 mutation;Albrecht;Am J Med Genet A,2004
3. Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy;Kohlhase;J Med Genet,2003
4. Embryonic expression of the murine homologue of SALL1, the gene mutated in Townes--Brocks syndrome;Buck;Mech Dev,2001
5. Familial transmission of oculoauriculovertebral spectrum (Goldenhar syndrome) is not due to mutations in either EYA1 or SALL1;Goodin;Am J Med Genet A,2009
Cited by
4 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