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Journal Abstract Search
103 related items for PubMed ID: 4039896
21. The unilateral stapes gusher. Rebol J. Wien Klin Wochenschr; 2004; 116 Suppl 2():90-2. PubMed ID: 15506322 [Abstract] [Full Text] [Related]
23. X-linked mixed hearing loss with stapes fixation: case reports. Carlson DL, Reeh HL. J Am Acad Audiol; 1993 Nov; 4(6):420-5. PubMed ID: 8298178 [Abstract] [Full Text] [Related]
24. Fragile X chromosome and X-linked mental retardation. Larbrisseau A, Jean P, Messier B, Richer CL. Can Med Assoc J; 1982 Jul 15; 127(2):123-6. PubMed ID: 7093857 [Abstract] [Full Text] [Related]
25. [Marshall syndrome. 2 new cases]. Nguyen J, Philip N, Arnaud JP, Sibille G, Tisne C, James F. Arch Fr Pediatr; 1988 Jan 15; 45(1):49-51. PubMed ID: 3365105 [Abstract] [Full Text] [Related]
26. [Rupture of the membrane of the round window in stapes fixation]. Gungl M, Bauer M. HNO; 1987 Nov 15; 35(11):482-4. PubMed ID: 3692935 [Abstract] [Full Text] [Related]
27. Noninvasive assessment of the intralabyrinthine pressure. A new technique applied to patients with X-linked progressive mixed deafness syndrome with perilymphatic gusher during stapes surgery. Ernst A, Snik FM, Mylanus IA, Cremers WR. Arch Otolaryngol Head Neck Surg; 1995 Aug 15; 121(8):926-9. PubMed ID: 7619423 [Abstract] [Full Text] [Related]
29. Oto-palatal-digital syndrome type II with X-linked cerebellar hypoplasia/hydrocephalus. Stratton RF, Bluestone DL. Am J Med Genet; 1991 Nov 01; 41(2):169-72. PubMed ID: 1785627 [Abstract] [Full Text] [Related]
36. [Clinical and molecular genetic analysis of monozygotic twins displaying stapes gusher syndrome (DFN3)]. Oh N, Kupka S, Mirghomizadeh F, Arold R, Zimmermann R, Blin N, Zenner HP, Pfister M. HNO; 2003 Aug 01; 51(8):629-33. PubMed ID: 12942177 [Abstract] [Full Text] [Related]
37. [Norrie-Wardburg syndrome]. Skevas A, Kastanioudakis I, Daniilidis B, Exarchakos G. Laryngorhinootologie; 1992 Oct 01; 71(10):534-6. PubMed ID: 1418232 [Abstract] [Full Text] [Related]
38. Phenotype and genotype in females with POU3F4 mutations. Marlin S, Moizard MP, David A, Chaissang N, Raynaud M, Jonard L, Feldmann D, Loundon N, Denoyelle F, Toutain A. Clin Genet; 2009 Dec 01; 76(6):558-63. PubMed ID: 19930154 [Abstract] [Full Text] [Related]
40. Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21. Merry DE, Lesko JG, Sosnoski DM, Lewis RA, Lubinsky M, Trask B, van den Engh G, Collins FS, Nussbaum RL. Am J Hum Genet; 1989 Oct 01; 45(4):530-40. PubMed ID: 2491012 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]