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4. Conductive hearing loss and malformed low-set ears, as a possible recessive syndrome. Mengel MC; Konigsmark BW; Berlin CI; McKusick VA J Med Genet; 1969 Mar; 6(1):14-21. PubMed ID: 5771216 [No Abstract] [Full Text] [Related]
5. Genetic hearing loss with no associated abnormalities: a review. Konigsmark BW J Speech Hear Disord; 1972 Feb; 37(1):89-99. PubMed ID: 4559857 [No Abstract] [Full Text] [Related]
6. Reliability of Békésy threshold tracing in identification of carriers of genes for an X-linked disease with deafness. Parving A Acta Otolaryngol; 1978; 85(1-2):40-4. PubMed ID: 626054 [TBL] [Abstract][Full Text] [Related]
7. Usher's syndrome--deafness and progressive blindness. Clinical cases, prevention, theory and literature survey. Vernon M J Chronic Dis; 1969 Aug; 22(3):133-51. PubMed ID: 4897966 [No Abstract] [Full Text] [Related]
10. Recessive sex-linked mental retardation in the absence of other recognizable abnormalities. Report of a family. Snyder RD; Robinson A Clin Pediatr (Phila); 1969 Nov; 8(11):669-74. PubMed ID: 5823961 [No Abstract] [Full Text] [Related]
11. X-linked deafness in a South African kindred. Thorpe P; Sellars S; Beighton P S Afr Med J; 1974 Mar; 48(14):587-90. PubMed ID: 4821674 [No Abstract] [Full Text] [Related]
12. Deafness, onycho-osteodystrophy, mental retardation (DOOR) syndrome. Nevin NC; Thomas PS; Calvert J; Reid MM Am J Med Genet; 1982 Nov; 13(3):325-32. PubMed ID: 7180877 [No Abstract] [Full Text] [Related]
13. Choroideremia, congenital deafness and mental retardation in a family with an X chromosomal deletion. Rosenberg T; Niebuhr E; Yang HM; Parving A; Schwartz M Ophthalmic Paediatr Genet; 1987 Nov; 8(3):139-43. PubMed ID: 3438052 [TBL] [Abstract][Full Text] [Related]
14. A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22. Tranebjaerg L; Schwartz C; Eriksen H; Andreasson S; Ponjavic V; Dahl A; Stevenson RE; May M; Arena F; Barker D J Med Genet; 1995 Apr; 32(4):257-63. PubMed ID: 7643352 [TBL] [Abstract][Full Text] [Related]
15. Congenital deafness and hypogonadism: a new X-linked recessive disorder. Myhre SA; Ruvalcaba RH; Kelley VC Clin Genet; 1982 Dec; 22(6):299-307. PubMed ID: 6819099 [No Abstract] [Full Text] [Related]
16. A note on the detection of linkage of a possible X-linked locus to a known X-linked locus. Denniston C Am J Hum Genet; 1969 Sep; 21(5):419-22. PubMed ID: 5822289 [No Abstract] [Full Text] [Related]
18. X-linked mixed deafness with congenital fixation of the stapedial footplate and perilymphatic gusher. Nance WE; Setleff R; McLeod A; Sweeney A; Cooper C; McConnell F Birth Defects Orig Artic Ser; 1971 Mar; 07(4):64-9. PubMed ID: 5173351 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]