Author:
Ting Teck Wah,Lai Angeline Hwei Meeng,Choo Jonathan Tze Liang,Tan Teng Hong
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Reference12 articles.
1. Adès LC (2008) Evolution of the face in Loeys–Dietz syndrome type II: longitudinal observations from infancy in seven cases. Clin Dysmorphol 17(4):243–248
2. Akutsu K, Morisaki H, Takeshita S, Sakamoto S, Tamori Y, Yoshimuta T, Yokoyama N, Nonoqi H, Ogino H, Morisaki T (2007) Phenotypic heterogeneity of Marfan-like connective tissue disorder with mutations in the transforming growth factor receptor genes. Circ J 71:1305–1309
3. Kilic E, Alanay Y, Ütine E, Özgen-Mocan B, Robinson PN, Boduroğlu K (2012) Arterial tortuosity and aneurysm in a case of Loeys–Dietz syndrome type 1B with a mutation p.R537P in the TGFBR2 gene. Turk J Pediatr 54:198–202
4. Loeys BL, Chen J, Neptune ER, Judge DP, Podowski M, Holm T, Meyers J, Leitch CC, Katsanis N, Sharifi N, Xu FL, Myers LA, Spevak PJ, Cameron DE, De Backer J, Hellemans J, Chen Y, Davis EC, Webb CL, Kress W, Coucke P, Rifkin DB, De Paepe AM, Dietz HC (2005) A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2. Nat Genet 37:275–281
5. Loeys BL, Dietz HC. ( 2008, revised 2013) Loeys-Dietz Syndrome. In: Pagon RA, Adam MP, Bird TD, et al., editors. GeneReviews™ [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2013.
Cited by
1 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