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Journal Abstract Search
155 related items for PubMed ID: 1519658
1. Beare-Stevenson cutis gyrata syndrome. Hall BD, Cadle RG, Golabi M, Morris CA, Cohen MM. Am J Med Genet; 1992 Sep 01; 44(1):82-9. PubMed ID: 1519658 [Abstract] [Full Text] [Related]
2. Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome. Przylepa KA, Paznekas W, Zhang M, Golabi M, Bias W, Bamshad MJ, Carey JC, Hall BD, Stevenson R, Orlow S, Cohen MM, Jabs EW. Nat Genet; 1996 Aug 01; 13(4):492-4. PubMed ID: 8696350 [Abstract] [Full Text] [Related]
10. A Case of Beare-Stevenson Syndrome with Unusual Manifestations. Ron N, Leung S, Carney E, Gerber A, David KL. Am J Case Rep; 2016 Apr 15; 17():254-8. PubMed ID: 27079505 [Abstract] [Full Text] [Related]
11. Beare-Stevenson syndrome: two new patients, including a novel finding of tracheal cartilaginous sleeve. Wenger TL, Bhoj EJ, Wetmore RF, Mennuti MT, Bartlett SP, Mollen TJ, McDonald-McGinn DM, Zackai EH. Am J Med Genet A; 2015 Apr 15; 167A(4):852-7. PubMed ID: 25706251 [Abstract] [Full Text] [Related]
13. A case of Beare-Stevenson cutis gyrata syndrome confirmed by mutation analysis of the fibroblast growth factor receptor 2 gene. Akai T, Iizuka H, Kishibe M, Kawakami S, Kobayashi A, Ozawa T. Pediatr Neurosurg; 2002 Aug 15; 37(2):97-9. PubMed ID: 12145519 [Abstract] [Full Text] [Related]
17. Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis. Cohen MM. Am J Med Genet; 1993 Feb 01; 45(3):300-7. PubMed ID: 8434615 [Abstract] [Full Text] [Related]