Fraser Syndrome: Prenatal Detection at 16 Weeks of Gestation
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s40556-016-0081-3.pdf
Reference11 articles.
1. Francannet C, Lefrançois P, Dechelotte P, Robert E, Malpuech G, Robert JM. Fraser syndrome with renal agenesis in two consanguineous Turkish families. Am J Med Genet. 1990;36(4):477–9.
2. Narang M, Kumar M, Shah D. Fraser-cryptophthalmos syndrome with colonic atresia. Indian J Pediatr. 2008;75(2):189–91.
3. McGregor L, Makela V, Darling SM, Vrontou S, Chalepakis G, Roberts C, et al. Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein. Nat Genet. 2003;34(2):203–8.
4. Jadeja S, Smyth I, Pitera JE, Taylor MS, van Haelst M, Bentley E, et al. Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs. Nat Genet. 2005;37(5):520–5.
5. Vogel MJ, van Zon P, Brueton L, Gijzen M, van Tuil MC, Cox P, et al. Mutations in GRIP1 cause Fraser syndrome. J Med Genet. 2012;49(5):303–6.
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