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6. [Evaluation of a consultation on infants with deficient hearing over the course of three years: genetic aspects]. Bruneaud D; Gaillard de Collogny L; Lafaye M; Malpuech G J Genet Hum; 1976 Nov; 24 Suppl():199-206. PubMed ID: 1025271 [No Abstract] [Full Text] [Related]
7. Hearing impairment in female carriers of the sex-linked syndrome of deafness with albinism. Fried K; Feinmesser M; Tsitsianov J J Med Genet; 1969 Jun; 6(2):132-4. PubMed ID: 5801459 [No Abstract] [Full Text] [Related]
8. [Forms of monosymptomatic hereditary sensorineural hearing loss and deafness in the Leipzig area]. Oeken J; König E HNO; 1993 Jun; 41(6):301-10. PubMed ID: 8365917 [TBL] [Abstract][Full Text] [Related]
9. [Determination of difficulty of hearing grade and the restriction of hereditary ability in small children]. von Arentsschild O HNO; 1969 Mar; 17(3):86-9. PubMed ID: 5405365 [No Abstract] [Full Text] [Related]
12. [Association of genetic deafness and tranomission hypoacousia due to pharynogo-tympanic dysembryoma]. Desnos J; Martin A Ann Otolaryngol Chir Cervicofac; 1974; 91(7-8):411-6. PubMed ID: 4451328 [No Abstract] [Full Text] [Related]
14. [Modern concepts of the role of heredity in the origin of monosymptomatic hearing disorders in children]. Bliumina MG; Moskovkina AG Vestn Otorinolaringol; 1980; (1):67-73. PubMed ID: 6990581 [No Abstract] [Full Text] [Related]
15. [Hearing fatigue in Békésy audiometry as means of differential diagnosis]. Baldus S; Gastpar H HNO; 1970 Jun; 18(6):185-7. PubMed ID: 5514151 [No Abstract] [Full Text] [Related]
20. [Etiopathogenic and topofunctional study of the auditory deficit in deaf-mutes. Its value as a function of auditory rehabilitation]. López Martínez R Rev Esp Otoneurooftalmol Neurocir; 1966; 25(145):219-30 contd. PubMed ID: 5974364 [No Abstract] [Full Text] [Related] [Next] [New Search]