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.
30. Subclinical audiological findings in carriers of recessive genes for deafness. Berlin M; Legum C; Muchnik C; Hildesheimer M J Basic Clin Physiol Pharmacol; 1999; 10(3):201-8. PubMed ID: 10529906 [TBL] [Abstract][Full Text] [Related]
31. Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families. Deng Y; Sang S; Wen J; Liu Y; Ling J; Chen H; Cai X; Mei L; Chen X; Li M; Li W; Li T; He C; Feng Y Int J Pediatr Otorhinolaryngol; 2018 Dec; 115():114-119. PubMed ID: 30368370 [TBL] [Abstract][Full Text] [Related]
32. [Genetic counseling]. Klein D Bull Schweiz Akad Med Wiss; 1972 Sep; 28(5):250-65. PubMed ID: 4566685 [No Abstract] [Full Text] [Related]
33. [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]
34. The genetics of sensorineural deafness. McGill JJ Med J Aust; 1991 May; 154(9):572-4. PubMed ID: 2056938 [No Abstract] [Full Text] [Related]
35. Autosomal recessive nonsyndromal profound childhood deafness in a large pedigree. Audiometric features of the affected persons and the obligate carriers. Marres HA; Cremers CW Arch Otolaryngol Head Neck Surg; 1989 May; 115(5):591-5. PubMed ID: 2706105 [TBL] [Abstract][Full Text] [Related]
36. [The significance of genetic factors in epilepsies]. Moser H Schweiz Rundsch Med Prax; 1985 Jun; 74(24):636-42. PubMed ID: 4023499 [No Abstract] [Full Text] [Related]
38. Identification of normal hearing carriers of genes for deafness. Anderson H; Wedenberg E Acta Otolaryngol; 1976; 82(3-4):245-8. PubMed ID: 983683 [TBL] [Abstract][Full Text] [Related]
39. [Diagnosis of malformations of the ear and temporal bone]. Terrahe K Arch Klin Exp Ohren Nasen Kehlkopfheilkd; 1972; 202(1):85-151. PubMed ID: 5032730 [No Abstract] [Full Text] [Related]
40. Recurrence risks for near relatives of children with sensori-neural deafness. Koehn D; Morgan K; Fraser FC Genet Couns; 1990; 1(2):127-32. PubMed ID: 2080997 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]