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Brachmann-de Lange syndrome with normal IQ.
Saal HM, Samango-Sprouse CA, Rodnan LA, Rosenbaum KN, Custer DA. Saal HM, et al. Am J Med Genet. 1993 Nov 15;47(7):995-8. doi: 10.1002/ajmg.1320470711. Am J Med Genet. 1993. PMID: 8291543 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. Among authors: saal hm. Am J Med Genet. 1997 Jun 27;70(4):377-86. Am J Med Genet. 1997. PMID: 9182778 Review.
Middle ear disease in childhood achondroplasia.
Berkowitz RG, Grundfast KM, Scott C, Saal H, Stern H, Rosenbaum K. Berkowitz RG, et al. Ear Nose Throat J. 1991 May;70(5):305-8. Ear Nose Throat J. 1991. PMID: 1914954 No abstract available.
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
135 results