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SEMA3E mutation in a patient with CHARGE syndrome.
Lalani SR, Safiullah AM, Molinari LM, Fernbach SD, Martin DM, Belmont JW. Lalani SR, et al. Among authors: molinari lm. J Med Genet. 2004 Jul;41(7):e94. doi: 10.1136/jmg.2003.017640. J Med Genet. 2004. PMID: 15235037 Free PMC article. No abstract available.
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: molinari lm. BMC Med Genet. 2005 Feb 14;6:8. doi: 10.1186/1471-2350-6-8. BMC Med Genet. 2005. PMID: 15710038 Free PMC article.
Melanoma With Meyerson's Phenomenon: Clinical and Dermoscopic Features.
Bollea-Garlatti LA, Molinari LM, Galimberti GN, Galimberti RL. Bollea-Garlatti LA, et al. Among authors: molinari lm. Actas Dermosifiliogr. 2016 Apr;107(3):255-7. doi: 10.1016/j.ad.2015.06.013. Epub 2015 Nov 3. Actas Dermosifiliogr. 2016. PMID: 26546031 Free article. English, Spanish. No abstract available.
11 results