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Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.
Ensenauer RE, Adeyinka A, Flynn HC, Michels VV, Lindor NM, Dawson DB, Thorland EC, Lorentz CP, Goldstein JL, McDonald MT, Smith WE, Simon-Fayard E, Alexander AA, Kulharya AS, Ketterling RP, Clark RD, Jalal SM. Ensenauer RE, et al. Among authors: michels vv. Am J Hum Genet. 2003 Nov;73(5):1027-40. doi: 10.1086/378818. Epub 2003 Oct 2. Am J Hum Genet. 2003. PMID: 14526392 Free PMC article.
Delineation of the cryptic 1qter deletion phenotype.
Merritt JL 2nd, Zou Y, Jalal SM, Michels VV. Merritt JL 2nd, et al. Among authors: michels vv. Am J Med Genet A. 2007 Mar 15;143A(6):599-603. doi: 10.1002/ajmg.a.31611. Am J Med Genet A. 2007. PMID: 17304549
Uniparental disomy in congenital disorders: a prospective study.
Lindor NM, Karnes PS, Michels VV, Dewald GW, Goerss J, Jalal S, Jenkins RB, Vockley G, Thibodeau SN. Lindor NM, et al. Among authors: michels vv. Am J Med Genet. 1995 Aug 28;58(2):143-6. doi: 10.1002/ajmg.1320580210. Am J Med Genet. 1995. PMID: 8533805
Cytogenetic testing for Williams syndrome.
Jalal SM, Crifasi PA, Karnes PS, Michels VV. Jalal SM, et al. Among authors: michels vv. Mayo Clin Proc. 1996 Jan;71(1):67-8. doi: 10.4065/71.1.67. Mayo Clin Proc. 1996. PMID: 8538237 No abstract available.
136 results