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Terminal deletion of 6p results in a recognizable phenotype.
Lin RJ, Cherry AM, Chen KC, Lyons M, Hoyme HE, Hudgins L. Lin RJ, et al. Among authors: cherry am. Am J Med Genet A. 2005 Jul 15;136(2):162-8. doi: 10.1002/ajmg.a.30784. Am J Med Genet A. 2005. PMID: 15940702 Review.
A report of three patients with an interstitial deletion of chromosome 15q24.
Cushman LJ, Torres-Martinez W, Cherry AM, Manning MA, Abdul-Rahman O, Anderson CE, Punnett HH, Thurston VC, Sweeney D, Vance GH. Cushman LJ, et al. Among authors: cherry am. Am J Med Genet A. 2005 Aug 15;137(1):65-71. doi: 10.1002/ajmg.a.30836. Am J Med Genet A. 2005. PMID: 16007617 Review.
Acute leukemia in a patient with 15q overgrowth syndrome.
Bodle EE, Gupta R, Cherry AM, Muffly L, Manning MA. Bodle EE, et al. Among authors: cherry am. Am J Med Genet A. 2019 Jun;179(6):1025-1029. doi: 10.1002/ajmg.a.61115. Epub 2019 Mar 12. Am J Med Genet A. 2019. PMID: 30861314
Perinatal distress in 1p36 deletion syndrome can mimic hypoxic ischemic encephalopathy.
Carter LB, Battaglia A, Cherry A, Manning MA, Ruzhnikov MR, Bird LM, Dowsett L, Graham JM Jr, Alkuraya FS, Hashem M, Dinulos MB, Vallee S, Adam MP, Glass I, Beck AE, Stevens CA, Zackai E, McDougall C, Keena B, Peron A, Vignoli A, Seaver LH, Slavin TP, Hudgins L. Carter LB, et al. Am J Med Genet A. 2019 Aug;179(8):1543-1546. doi: 10.1002/ajmg.a.61266. Epub 2019 Jun 17. Am J Med Genet A. 2019. PMID: 31207089 Free PMC article. Review.
88 results