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Items: 4

1.
Retinoid Signaling in Inner Ear Development: a “Goldilocks” Phenomenon
Dorothy A. Frenz, Wei Liu, Ales Cvekl, Qing Xie, Lesley Wassef, Loredana Quadro, Karen Niederreither, Mark Maconochie, Alan Shanske
Am J Med Genet A. Author manuscript; available in PMC 2011 Dec 1.
Published in final edited form as: Am J Med Genet A. 2010 Dec; 152A(12): 2947–2961. doi: 10.1002/ajmg.a.33670
PMCID:
PMC3057869
AbstractArticlePDF–1.8M
2.
Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3)
Osama Alsmadi, Brian F Meyer, Fowzan Alkuraya, Salma Wakil, Fadi Alkayal, Haya Al-Saud, Khushnooda Ramzan, MoeenAldeen Al-Sayed
Eur J Hum Genet. 2009 Jan; 17(1): 14–21. Published online 2008 Aug 13. doi: 10.1038/ejhg.2008.141
PMCID:
PMC2985964
AbstractArticlePDF–310K
3.
Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia
Mustafa  Tekin, Burcu Öztürk  Hişmi, Suat  Fitoz, Hilal  Özdağ, Filiz Başak  Cengiz, Aslı  Sırmacı, İdil  Aslan, Bora  İnceoğlu, E. Berrin  Yüksel-Konuk, Seda Taşır  Yılmaz, Öztan  Yasun, Nejat  Akar
Am J Hum Genet. 2007 Feb; 80(2): 338–344. Published online 2006 Dec 27. doi: 10.1086/510920
PMCID:
PMC1785350
AbstractArticlePDF–1.3M
4.
Characterization and chromosome assignment of the human homolog of int-2, a potential proto-oncogene.
G Casey, R Smith, D McGillivray, G Peters, C Dickson
Mol Cell Biol. 1986 Feb; 6(2): 502–510. doi: 10.1128/mcb.6.2.502
PMCID:
PMC367539
SummaryPage BrowsePDF–1.8M

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