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Challenging the status quo of scientific presentations.
Chatterjee D, Yaster M, Lockman JL, Glass NL, Schreiner MS, Sinskey JL, Fiadjoe JE. Chatterjee D, et al. Among authors: glass nl. Paediatr Anaesth. 2021 Feb;31(2):116-122. doi: 10.1111/pan.14064. Epub 2020 Nov 20. Paediatr Anaesth. 2021. PMID: 33151606
Congenital Cardiac Anesthesia Society meeting review.
Glass NL, Valley RD; Congenital Cardiac Anesthesia Society. Glass NL, et al. Anesth Analg. 2007 Oct;105(4):974-6. doi: 10.1213/01.ane.0000278632.22988.d7. Anesth Analg. 2007. PMID: 17898375 No abstract available.
Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.
Lalani SR, Safiullah AM, Fernbach SD, Harutyunyan KG, Thaller C, Peterson LE, McPherson JD, Gibbs RA, White LD, Hefner M, Davenport SL, Graham JM, Bacino CA, Glass NL, Towbin JA, Craigen WJ, Neish SR, Lin AE, Belmont JW. Lalani SR, et al. Among authors: glass nl. Am J Hum Genet. 2006 Feb;78(2):303-14. doi: 10.1086/500273. Epub 2005 Dec 29. Am J Hum Genet. 2006. PMID: 16400610 Free PMC article.
SNP genotyping to screen for a common deletion in CHARGE syndrome.
Lalani SR, Safiullah AM, Fernbach SD, Phillips M, Bacino CA, Molinari LM, Glass NL, Towbin JA, Craigen WJ, Belmont JW. Lalani SR, et al. Among authors: glass nl. BMC Med Genet. 2005 Feb 14;6:8. doi: 10.1186/1471-2350-6-8. BMC Med Genet. 2005. PMID: 15710038 Free PMC article.
185 results