Morton CC - Search Results

1

The Burden and Benefits of Knowledge: Ethical Considerations Surrounding Population-Based Newborn Genome Screening for Hearing.

Mitchell CO, Rivera-Cruz G, Chau MHK, Dong Z, Choy KW, Shen J, Amr S, Giersch ABS, Morton CC. Mitchell CO, et al. Among authors: morton cc. Int J Neonatal Screen. 2022 May 27;8(2):36. doi: 10.3390/ijns8020036. Int J Neonatal Screen. 2022. PMID: 35735787 Free PMC article.

2

Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss.

Stover EH, Borthwick KJ, Bavalia C, Eady N, Fritz DM, Rungroj N, Giersch AB, Morton CC, Axon PR, Akil I, Al-Sabban EA, Baguley DM, Bianca S, Bakkaloglu A, Bircan Z, Chauveau D, Clermont MJ, Guala A, Hulton SA, Kroes H, Li Volti G, Mir S, Mocan H, Nayir A, Ozen S, Rodriguez Soriano J, Sanjad SA, Tasic V, Taylor CM, Topaloglu R, Smith AN, Karet FE. Stover EH, et al. Among authors: morton cc. J Med Genet. 2002 Nov;39(11):796-803. doi: 10.1136/jmg.39.11.796. J Med Genet. 2002. PMID: 12414817 Free PMC article.

3

Isolation from cochlea of a novel human intronless gene with predominant fetal expression.

Resendes BL, Kuo SF, Robertson NG, Giersch AB, Honrubia D, Ohara O, Adams JC, Morton CC. Resendes BL, et al. Among authors: morton cc. J Assoc Res Otolaryngol. 2004 Jun;5(2):185-202. doi: 10.1007/s10162-003-4042-x. J Assoc Res Otolaryngol. 2004. PMID: 15357420 Free PMC article.

4

Characterization of an abundant COL9A1 transcript in the cochlea with a novel 3' UTR: Expression studies and detection of miRNA target sequence.

Sivakumaran TA, Resendes BL, Robertson NG, Giersch AB, Morton CC. Sivakumaran TA, et al. Among authors: morton cc. J Assoc Res Otolaryngol. 2006 Jun;7(2):160-72. doi: 10.1007/s10162-006-0032-0. Epub 2006 Apr 19. J Assoc Res Otolaryngol. 2006. PMID: 16718610 Free PMC article.

5

Ion channel gene expression in the inner ear.

Gabashvili IS, Sokolowski BH, Morton CC, Giersch AB. Gabashvili IS, et al. Among authors: morton cc. J Assoc Res Otolaryngol. 2007 Sep;8(3):305-28. doi: 10.1007/s10162-007-0082-y. Epub 2007 Jun 1. J Assoc Res Otolaryngol. 2007. PMID: 17541769 Free PMC article.

6

Expression studies of osteoglycin/mimecan (OGN) in the cochlea and auditory phenotype of Ogn-deficient mice.

Williamson RE, Darrow KN, Giersch AB, Resendes BL, Huang M, Conrad GW, Chen ZY, Liberman MC, Morton CC, Tasheva ES. Williamson RE, et al. Among authors: morton cc. Hear Res. 2008 Mar;237(1-2):57-65. doi: 10.1016/j.heares.2007.12.006. Epub 2007 Dec 28. Hear Res. 2008. PMID: 18243607 Free PMC article.

7

Reporting of diagnostic cytogenetic results.

Ligon AH, Morton CC, Bieber FR, Fletcher JA, Giersch AB, Lee C, Sandstrom M, Weremowicz S, Xiao S, Dal Cin P. Ligon AH, et al. Among authors: morton cc. Curr Protoc Hum Genet. 2004 Nov;Appendix 1:Appendix 1D. doi: 10.1002/0471142905.hga01ds43. Curr Protoc Hum Genet. 2004. PMID: 18428350

8

A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction.

Robertson NG, Jones SM, Sivakumaran TA, Giersch AB, Jurado SA, Call LM, Miller CE, Maison SF, Liberman MC, Morton CC. Robertson NG, et al. Among authors: morton cc. Hum Mol Genet. 2008 Nov 1;17(21):3426-34. doi: 10.1093/hmg/ddn236. Epub 2008 Aug 12. Hum Mol Genet. 2008. PMID: 18697796 Free PMC article.

9

Disseminated peritoneal leiomyomatosis after laparoscopic supracervical hysterectomy with characteristic molecular cytogenetic findings of uterine leiomyoma.

Ordulu Z, Dal Cin P, Chong WW, Choy KW, Lee C, Muto MG, Quade BJ, Morton CC. Ordulu Z, et al. Among authors: morton cc. Genes Chromosomes Cancer. 2010 Dec;49(12):1152-60. doi: 10.1002/gcc.20824. Genes Chromosomes Cancer. 2010. PMID: 20842731 Free PMC article.

10

Reporting of diagnostic cytogenetic results.

Ligon AH, Morton CC, Bieber FR, Fletcher JA, Giersch AB, Kantarci S, Leach N, Lee C, Sandstrom M, Weremowicz S, Xiao S, Dal Cin P. Ligon AH, et al. Among authors: morton cc. Curr Protoc Hum Genet. 2010 Oct;Appendix 1:1D.1-23. doi: 10.1002/0471142905.hga01ds67. Curr Protoc Hum Genet. 2010. PMID: 20891028

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