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Long-term survival in a patient with del(18)(q12.2q21.1).
Tinkle BT, Christianson CA, Schorry EK, Webb T, Hopkin RJ. Tinkle BT, et al. Among authors: schorry ek. Am J Med Genet A. 2003 May 15;119A(1):66-70. doi: 10.1002/ajmg.a.10217. Am J Med Genet A. 2003. PMID: 12707962
Familial partial duplication (1)(p21p31).
Hoechstetter L, Soukup S, Schorry EK. Hoechstetter L, et al. Among authors: schorry ek. Am J Med Genet. 1995 Nov 20;59(3):291-4. doi: 10.1002/ajmg.1320590305. Am J Med Genet. 1995. PMID: 8599351 Review.
New insights into the phenotypes of 6q deletions.
Hopkin RJ, Schorry E, Bofinger M, Milatovich A, Stern HJ, Jayne C, Saal HM. Hopkin RJ, et al. Am J Med Genet. 1997 Jun 27;70(4):377-86. Am J Med Genet. 1997. PMID: 9182778 Review.
Human blood genomics: distinct profiles for gender, age and neurofibromatosis type 1.
Tang Y, Lu A, Ran R, Aronow BJ, Schorry EK, Hopkin RJ, Gilbert DL, Glauser TA, Hershey AD, Richtand NW, Privitera M, Dalvi A, Sahay A, Szaflarski JP, Ficker DM, Ratner N, Sharp FR. Tang Y, et al. Among authors: schorry ek. Brain Res Mol Brain Res. 2004 Dec 20;132(2):155-67. doi: 10.1016/j.molbrainres.2003.10.014. Brain Res Mol Brain Res. 2004. PMID: 15582155
Epidemiology of hemimegalencephaly: a case series and review.
Tinkle BT, Schorry EK, Franz DN, Crone KR, Saal HM. Tinkle BT, et al. Among authors: schorry ek. Am J Med Genet A. 2005 Dec 15;139(3):204-11. doi: 10.1002/ajmg.a.31024. Am J Med Genet A. 2005. PMID: 16283674 Review.
76 results