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Klippel-Trenaunay syndrome.
Berry SA, Peterson C, Mize W, Bloom K, Zachary C, Blasco P, Hunter D. Berry SA, et al. Am J Med Genet. 1998 Oct 2;79(4):319-26. Am J Med Genet. 1998. PMID: 9781914 Review.
Cockayne syndrome: review of 140 cases.
Nance MA, Berry SA. Nance MA, et al. Among authors: berry sa. Am J Med Genet. 1992 Jan 1;42(1):68-84. doi: 10.1002/ajmg.1320420115. Am J Med Genet. 1992. PMID: 1308368 Review.
Neuroblastoma in a patient with Sotos' syndrome.
Nance MA, Neglia JP, Talwar D, Berry SA. Nance MA, et al. Among authors: berry sa. J Med Genet. 1990 Feb;27(2):130-2. doi: 10.1136/jmg.27.2.130. J Med Genet. 1990. PMID: 2319581 Free PMC article.
Brain anomalies, retardation of mentality and growth, ectodermal dysplasia, skeletal malformations, Hirschsprung disease, ear deformity and deafness, eye hypoplasia, cleft palate, cryptorchidism, and kidney dysplasia/hypoplasia (BRESEK/BRESHECK): new X-linked syndrome?
Reish O, Gorlin RJ, Hordinsky M, Rest EB, Burke B, Berry SA. Reish O, et al. Among authors: berry sa. Am J Med Genet. 1997 Feb 11;68(4):386-90. doi: 10.1002/(sici)1096-8628(19970211)68:4<386::aid-ajmg2>3.0.co;2-k. Am J Med Genet. 1997. PMID: 9021007
A novel microdeletion/microduplication syndrome of 19p13.13.
Dolan M, Mendelsohn NJ, Pierpont ME, Schimmenti LA, Berry SA, Hirsch B. Dolan M, et al. Among authors: berry sa. Genet Med. 2010 Aug;12(8):503-11. doi: 10.1097/GIM.0b013e3181e59291. Genet Med. 2010. PMID: 20613546 Free article.
280 results