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Apert's syndrome journal articles from PubMed MEDLINE database

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Thurston A 
Vital endowments: Sir Charles Bell and the history of some congenital abnormalities of the upper limb. [Journal Article]
ANZ J Surg 2011 Dec; 81(12):900-4.
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Oberoi S, Hoffman WY, Vargervik K 
Craniofacial team management in Apert syndrome. [Journal Article]
Am J Orthod Dentofacial Orthop 2012 Apr; 141(4 Suppl):S82-7.
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Eijkenboom DF, Verbist BM, Cremers CW, et al. 
Bilateral conductive hearing impairment with hyperostosis of the temporal bone: a new finding in Robinow syndrome. [Case Reports, Journal Article]
Arch Otolaryngol Head Neck Surg 2012 Mar; 138(3):309-12.
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Xue G, Hemmings BA 
Phosphorylation of basic helix-loop-helix transcription factor Twist in development and disease. [Journal Article, Research Support, Non-U.S. Gov't, Review]
Biochem Soc Trans 2012 Feb; 40(1):90-3.
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Meazzini MC, Allevia F, Mazzoleni F, et al. 
Long-term follow-up of syndromic craniosynostosis after Le Fort III halo distraction: a cephalometric and CT evaluation. [Journal Article]
J Plast Reconstr Aesthet Surg 2012 Apr; 65(4):464-72.
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Harvey I, Brown S, Ayres O, et al. 
The Apert hand--angiographic planning of a single-stage, 5-digit release for all classes of deformity. [Journal Article]
J Hand Surg Am 2012 Jan; 37(1):152-8.
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Warren SM, Shetye PR, Obaid SI, et al. 
Long-term evaluation of midface position after Le Fort III advancement: a 20-plus-year follow-up. [Journal Article]
Plast Reconstr Surg 2012 Jan; 129(1):234-42.
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Selbst SM, Baghdassarian A 
Pediatric emergency medicine: legal briefs. [Case Reports, Journal Article, Legal Cases]
Pediatr Emerg Care 2011 Dec; 27(12):1213-5.
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Martínez-Abadías N, Heuzé Y, Wang Y, et al. 
FGF/FGFR signaling coordinates skull development by modulating magnitude of morphological integration: evidence from Apert syndrome mouse models. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
PLoS One 2011; 6(10):e26425.
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Zung A, Petek E, Ben-Zeev B, et al. 
MODY type 2 in Greig cephalopolysyndactyly syndrome (GCPS) as part of a contiguous gene deletion syndrome. [Journal Article]
Am J Med Genet A 2011 Oct; 155A(10):2469-72.
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