Author:
Alzahrani Fatema,Al Hazzaa Selwa A.,Tayeb Hamsa,Alkuraya Fowzan S.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference6 articles.
1. Alkuraya FS (2013) The application of next-generation sequencing in the autozygosity mapping of human recessive diseases. Hum Genet 132:1197–1211
2. Evans AK, Rahbar R, Rogers GF, Mulliken JB, Volk MS (2006) Robin sequence: a retrospective review of 115 patients. Int J Pediatr Otorhinolaryngol 70:973–980
3. Lee J-E, Kim Y (2006) A tissue-specific variant of the human lysyl oxidase-like protein 3 (LOXL3) functions as an amine oxidase with substrate specificity. J Biol Chem 281:37282–37290
4. Lucero H, Kagan H (2006) Lysyl oxidase: an oxidative enzyme and effector of cell function. Cell Mol Life Sci CMLS 63:2304–2316
5. Robin NH, Moran RT, Ala-Kokko L (2014) Stickler Syndrome. In: Pagon RA, Adam MP, Ardinger HH et al (eds) GeneReviews(r) [Internet], 1993–2015. University of Washington, Seattle. http://www.ncbi.nlm.nih.gov/books/NBK1302/
Cited by
58 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