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Familial laryngeal paralysis.
Manaligod JM, Smith RJ. Manaligod JM, et al. Among authors: smith rj. Am J Med Genet. 1998 May 26;77(4):277-80. doi: 10.1002/(sici)1096-8628(19980526)77:4<277::aid-ajmg5>3.0.co;2-k. Am J Med Genet. 1998. PMID: 9600735
Presymptomatic diagnosis of nonsyndromic hearing loss by genotyping.
Chen AH, Mueller RF, Prasad SD, Greinwald JH Jr, Manaligod J, Muilenburg AC, Verhoeven K, Van Camp G, Smith RJ. Chen AH, et al. Among authors: smith rj. Arch Otolaryngol Head Neck Surg. 1998 Jan;124(1):20-4. doi: 10.1001/archotol.124.1.20. Arch Otolaryngol Head Neck Surg. 1998. PMID: 9440775 Review.
Unilateral laryngeal dysgenesis.
Bent JP 3rd, Manaligod J, Smith RJ. Bent JP 3rd, et al. Among authors: smith rj. Otolaryngol Head Neck Surg. 1998 Dec;119(6):712. doi: 10.1016/S0194-5998(98)70044-0. Otolaryngol Head Neck Surg. 1998. PMID: 9852558 No abstract available.
Age-related mitochondrial DNA mutations in the human larynx.
Manaligod JM, Milam M, Hill SA, Sanders T, Skaggs J, Smith RJ. Manaligod JM, et al. Among authors: smith rj. Laryngoscope. 2000 Dec;110(12):2123-7. doi: 10.1097/00005537-200012000-00029. Laryngoscope. 2000. PMID: 11129034
Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21.
Greinwald JH Jr, Scott DA, Marietta JR, Carmi R, Manaligod J, Ramesh A, Zbar RI, Kraft ML, Elbedour K, Yairi Y, Musy M, Skvorak AB, Van Camp G, Srisailapathy CR, Lovett M, Morton CC, Sheffield VC, Smith RJ. Greinwald JH Jr, et al. Among authors: smith rj. Genome Res. 1997 Sep;7(9):879-86. doi: 10.1101/gr.7.9.879. Genome Res. 1997. PMID: 9314493 Free article.
Congenital laryngeal webs: surgical course and outcomes.
Goudy S, Bauman N, Manaligod J, Smith RJ. Goudy S, et al. Among authors: smith rj. Ann Otol Rhinol Laryngol. 2010 Oct;119(10):704-6. doi: 10.1177/000348941011901010. Ann Otol Rhinol Laryngol. 2010. PMID: 21049857
2,295 results