These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
95 related items for PubMed ID: 6789283
1. Heredity hearing losses with delayed onset: mechanisms of expression. Jahn AF, Noyek AM. Otolaryngol Clin North Am; 1981 Feb; 14(1):59-64. PubMed ID: 6789283 [Abstract] [Full Text] [Related]
2. Hearing loss is a common feature of symptomatic children with profound biotinidase deficiency. Wolf B, Spencer R, Gleason T. J Pediatr; 2002 Feb; 140(2):242-6. PubMed ID: 11865279 [Abstract] [Full Text] [Related]
3. [Modern concepts of the role of heredity in the origin of monosymptomatic hearing disorders in children]. Bliumina MG, Moskovkina AG. Vestn Otorinolaringol; 1980 Feb; (1):67-73. PubMed ID: 6990581 [No Abstract] [Full Text] [Related]
4. Hearing loss associated with hereditary diseases and syndromes. Sataloff RT. Ear Nose Throat J; 1983 Nov; 62(11):571-93. PubMed ID: 6360648 [No Abstract] [Full Text] [Related]
5. Hearing loss. Vernon M, Griffin DH, Yoken C. J Fam Pract; 1981 Jun; 12(6):1053-8. PubMed ID: 7229589 [Abstract] [Full Text] [Related]
17. [Early diagnosis important in hearing loss in children]. Hanner P. Nord Med; 1995 Oct 18; 110(10):261-3. PubMed ID: 7478966 [Abstract] [Full Text] [Related]