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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

71 related articles for article (PubMed ID: 4665370)

  • 1. [Familial forms of deafness].
    Gapanovich VIa; Timoshenko PA; Gorbachuk VD; Kachan AA; Lipnitskaia LN
    Vestn Otorinolaringol; 1972; 34(6):35-7. PubMed ID: 4665370
    [No Abstract]   [Full Text] [Related]  

  • 2. Familial low frequency hearing loss.
    Konigsmark BW; Mengel M; Berlin CI
    Laryngoscope; 1971 May; 81(5):759-71. PubMed ID: 5157378
    [No Abstract]   [Full Text] [Related]  

  • 3. The hereditary syndrome of congenital deafness and retinitis pigmentosa. (Usher's syndrome).
    Kloepfer HW; Laguaite JK
    Laryngoscope; 1966 May; 76(5):850-62. PubMed ID: 5937908
    [No Abstract]   [Full Text] [Related]  

  • 4. [Deafness and familial congenital auricular fistulas].
    Bailleul JP; Libersa C; Laude M
    Pediatrie; 1972; 27(7):739-47. PubMed ID: 4659974
    [No Abstract]   [Full Text] [Related]  

  • 5. [Etiological diagnosis of sensorineural deafness in children: a year-long review of genetic counseling for deaf people].
    Marlin S; Denoyelle F; Garabédian EN; Petit C
    Ann Otolaryngol Chir Cervicofac; 1998 Feb; 115(1):3-8. PubMed ID: 9765703
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [On some cases of familial congenital nephropathy with internal type deafness and lenticonus. (Clinical, anatomopathologic, pathogenetic and genealogic considerations)].
    Gambaro GC; Ravera M; Ciurlo G
    Arch Maragliano Patol Clin; 1966 Feb; 22(1):41-79. PubMed ID: 5952262
    [No Abstract]   [Full Text] [Related]  

  • 7. [Alport's syndrome or hereditary nephropathy with deafness. Further familial study].
    Burguet W; Lefebvre P; Booz G; Delwaide PJ; Van Cauwenberge H
    J Genet Hum; 1966 Jun; 15(1):7-20. PubMed ID: 5963517
    [No Abstract]   [Full Text] [Related]  

  • 8. Familial nephropathy and deafness: first observation of a family and close relatives in Switzerland.
    Dubach UC; Minder FC; Antener I
    Helv Med Acta; 1966 Apr; 33(1):36-43. PubMed ID: 5927986
    [No Abstract]   [Full Text] [Related]  

  • 9. [Pendred syndrome as a cause of familial deafness].
    Benito González J; Pérez Plasencia D; Benito González F; Blanco Pérez P; Aguirre García F; Mories T; Cañizo Alvarez A
    Acta Otorrinolaringol Esp; 1999; 50(6):477-9. PubMed ID: 10502702
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Familial hearing disorder with a hearing pattern of low-and-middle-tone losses].
    Kirikae I; Matsuzaki C; Hoshino T
    Jibiinkoka; 1968 Apr; 40(4):305-15. PubMed ID: 5748633
    [No Abstract]   [Full Text] [Related]  

  • 11. [Hearing disorders in school age children. Introduction. Statistics on causes of deafness in subjects in the Institute for Deaf-Mutes].
    Buondonno E; Pilotti G
    Minerva Med; 1972 Feb; 63(9):545-8. PubMed ID: 5010435
    [No Abstract]   [Full Text] [Related]  

  • 12. [Malformation of the 1st 2 branchial clefts and arches. Apropos of 8 familial cases comprising a particular syndrome].
    Bourguet J; Mazéas R; Lehuerou Y
    Ann Otolaryngol Chir Cervicofac; 1966; 83(4):317-27. PubMed ID: 5935940
    [No Abstract]   [Full Text] [Related]  

  • 13. [Morbidity and etiology of deaf-mutism in the province of Cadiz].
    Roquette Gaona J; Bartual Pastor J
    An Otorrinolaringol Ibero Am; 1982; 9(2):125-34. PubMed ID: 7091594
    [No Abstract]   [Full Text] [Related]  

  • 14. [Clinical study of juvenile unilateral deafness].
    Tsuiki T; Murai S
    J Comp Physiol Psychol; 1969 Nov; 69(3):540-1. PubMed ID: 5349042
    [No Abstract]   [Full Text] [Related]  

  • 15. [Selection of genes responsible for deafness].
    Kaneko S
    Nihon Jibiinkoka Gakkai Kaiho; 1970 Jul; 73(7):848-58. PubMed ID: 5465901
    [No Abstract]   [Full Text] [Related]  

  • 16. [On the impairment of the first 2 fissures and the first 2 brachial arches. (Apropos of 8 familial cases presenting an unusual syndrome)].
    Bourguet J; Mazeas R; Le Huérou Y
    Rev Otoneuroophtalmol; 1966; 38(4):161-75. PubMed ID: 5926353
    [No Abstract]   [Full Text] [Related]  

  • 17. [Familial cardio-auditory syndrome].
    Choussat A; Brousson R; Zebrowski A; Bricaud H
    Arch Mal Coeur Vaiss; 1970 Dec; 63(12):1715-27. PubMed ID: 4993651
    [No Abstract]   [Full Text] [Related]  

  • 18. Etiology of deafness in Robarts School for the Deaf.
    Janzen VD; Schaefer D
    J Otolaryngol; 1984 Feb; 13(1):47-8. PubMed ID: 6716551
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Associated anterior lenticonus, deafness and familial nephropathy(Alport's syndrome)].
    Ardouin M; Coutel Y; Bourguet J; Urvoy M; Thomet G
    J Genet Hum; 1966; 15():Suppl:44-8. PubMed ID: 4968158
    [No Abstract]   [Full Text] [Related]  

  • 20. [Hereditary progressive sensorineural deafness--report of 30 cases in 12 families].
    Wang X
    Zhonghua Yi Xue Za Zhi; 1983 Nov; 63(11):694-8. PubMed ID: 6426737
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.