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Items: 2

1.
Mutation analysis of Netrin 1 and HMX3 genes in patients with superior semicircular canal dehiscence syndrome
Nikola Roknic, Alexander Huber, Stefan C. A. Hegemann, Rudolf Häusler, Nicolas Gürtler
Acta Otolaryngol. 2012 Oct; 132(10): 1061–1065. Published online 2012 Jul 10. doi: 10.3109/00016489.2012.681797
PMCID:
PMC3477893
AbstractArticlePDF–167K
2.
Molecular (SNP) Analyses of Overlapping Hemizygous Deletions of 10q25.3 to 10qter in Four Patients: Evidence for HMX2 and HMX3 as Candidate Genes in Hearing and Vestibular Function
Nathaniel D. Miller, Melonie A. Nance, Elizabeth S. Wohler, Julie E. Hoover-Fong, Emily Lisi, George H. Thomas, Jonathan Pevsner
Am J Med Genet A. Author manuscript; available in PMC 2009 Sep 15.
Published in final edited form as: Am J Med Genet A. 2009 Feb 15; 149A(4): 669–680. doi: 10.1002/ajmg.a.32705
PMCID:
PMC2743949
AbstractArticlePDF–3.1M

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