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Growth hormone benefits children with 18q deletions.
Cody JD, Semrud-Clikeman M, Hardies LJ, Lancaster J, Ghidoni PD, Schaub RL, Thompson NM, Wells L, Cornell JE, Love TM, Fox PT, Leach RJ, Kaye CI, Hale DE. Cody JD, et al. Among authors: lancaster j. Am J Med Genet A. 2005 Aug 15;137(1):9-15. doi: 10.1002/ajmg.a.30848. Am J Med Genet A. 2005. PMID: 16007630
Narrowing critical regions and determining penetrance for selected 18q- phenotypes.
Cody JD, Heard PL, Crandall AC, Carter EM, Li J, Hardies LJ, Lancaster J, Perry B, Stratton RF, Sebold C, Schaub RL, Soileau B, Hill A, Hasi M, Fox PT, Hale DE. Cody JD, et al. Among authors: lancaster j. Am J Med Genet A. 2009 Jul;149A(7):1421-30. doi: 10.1002/ajmg.a.32899. Am J Med Genet A. 2009. PMID: 19533771 Free PMC article.
Tetrasomy 18p: report of the molecular and clinical findings of 43 individuals.
Sebold C, Roeder E, Zimmerman M, Soileau B, Heard P, Carter E, Schatz M, White WA, Perry B, Reinker K, O'Donnell L, Lancaster J, Li J, Hasi M, Hill A, Pankratz L, Hale DE, Cody JD. Sebold C, et al. Among authors: lancaster j. Am J Med Genet A. 2010 Sep;152A(9):2164-72. doi: 10.1002/ajmg.a.33597. Am J Med Genet A. 2010. PMID: 20803640
Consequences of chromsome18q deletions.
Cody JD, Sebold C, Heard P, Carter E, Soileau B, Hasi-Zogaj M, Hill A, Rupert D, Perry B, O'Donnell L, Gelfond J, Lancaster J, Fox PT, Hale DE. Cody JD, et al. Among authors: lancaster j. Am J Med Genet C Semin Med Genet. 2015 Sep;169(3):265-80. doi: 10.1002/ajmg.c.31446. Epub 2015 Aug 3. Am J Med Genet C Semin Med Genet. 2015. PMID: 26235940 Review.
Molecular characterization of a patient with central nervous system dysmyelination and cryptic unbalanced translocation between chromosomes 4q and 18q.
Gunn SR, Mohammed M, Reveles XT, Viskochil DH, Palumbos JC, Johnson-Pais TL, Hale DE, Lancaster JL, Hardies LJ, Boespflug-Tanguy O, Cody JD, Leach RJ. Gunn SR, et al. Among authors: lancaster jl. Am J Med Genet A. 2003 Jul 1;120A(1):127-35. doi: 10.1002/ajmg.a.20026. Am J Med Genet A. 2003. PMID: 12794705
Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome: evidence for myelin basic protein haploinsufficiency.
Gay CT, Hardies LJ, Rauch RA, Lancaster JL, Plaetke R, DuPont BR, Cody JD, Cornell JE, Herndon RC, Ghidoni PD, Schiff JM, Kaye CI, Leach RJ, Fox PT. Gay CT, et al. Among authors: lancaster jl. Am J Med Genet. 1997 Jul 25;74(4):422-31. doi: 10.1002/(sici)1096-8628(19970725)74:4<422::aid-ajmg14>3.0.co;2-k. Am J Med Genet. 1997. PMID: 9259379
A review of 18p deletions.
Hasi-Zogaj M, Sebold C, Heard P, Carter E, Soileau B, Hill A, Rupert D, Perry B, Atkinson S, O'Donnell L, Gelfond J, Lancaster J, Fox PT, Hale DE, Cody JD. Hasi-Zogaj M, et al. Among authors: lancaster j. Am J Med Genet C Semin Med Genet. 2015 Sep;169(3):251-64. doi: 10.1002/ajmg.c.31445. Epub 2015 Aug 6. Am J Med Genet C Semin Med Genet. 2015. PMID: 26250845
1,017 results