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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. Among authors: saal hm. Am J Med Genet. 1997 Jun 27;70(4):377-86. Am J Med Genet. 1997. PMID: 9182778 Review.
Ullrich-Turner syndrome and neurofibromatosis-1.
Schorry EK, Lovell AM, Milatovich A, Saal HM. Schorry EK, et al. Among authors: saal hm. Am J Med Genet. 1996 Dec 30;66(4):423-5. doi: 10.1002/(SICI)1096-8628(19961230)66:4<423::AID-AJMG6>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8989459
Epidemiology of hemimegalencephaly: a case series and review.
Tinkle BT, Schorry EK, Franz DN, Crone KR, Saal HM. Tinkle BT, et al. Among authors: saal hm. 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.
135 results