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Year | Number of Results |
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2005 | 1 |
2007 | 1 |
2013 | 1 |
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Orthodontic treatment of a patient with Stickler syndrome.
Angle Orthod. 2007 Sep;77(5):931-9. doi: 10.2319/082406-347.
Angle Orthod. 2007.
PMID: 17902239
Free article.
Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus.
Chen W, Kahrizi K, Meyer NC, Riazalhosseini Y, Van Camp G, Najmabadi H, Smith RJ.
Chen W, et al.
J Med Genet. 2005 Oct;42(10):e61. doi: 10.1136/jmg.2005.032615. Epub 2005 Jul 20.
J Med Genet. 2005.
PMID: 16033917
Free PMC article.
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Deletions within COL11A1 in Type 2 stickler syndrome detected by multiplex ligation-dependent probe amplification (MLPA).
Vijzelaar R, Waller S, Errami A, Donaldson A, Lourenco T, Rodrigues M, McConnell V, Fincham G, Snead M, Richards A.
Vijzelaar R, et al.
BMC Med Genet. 2013 Apr 26;14:48. doi: 10.1186/1471-2350-14-48.
BMC Med Genet. 2013.
PMID: 23621912
Free PMC article.
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