125 related articles for article (PubMed ID: 5771216)
1. 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]
2. Autosomal recessive sensorineural-conductive deafness, mental retardation, and pinna anomalies.
Cantú JM; Ruenes R; García-Cruz D
Hum Genet; 1978 Jan; 40(2):231-4. PubMed ID: 624552
[TBL] [Abstract][Full Text] [Related]
3. Metaphyseal dysostosis, conductive hearing loss and mental retardation: a recessively inherited syndrome.
Rimoin DL; McAlister WH
Birth Defects Orig Artic Ser; 1971 Mar; 07(4):116-22. PubMed ID: 5173335
[TBL] [Abstract][Full Text] [Related]
4. Familial infantile renal tubular acidosis and congenital nerve deafness: an autosomal recessive syndrome.
Cohen T; Brand-Auraban A; Karshai C; Jacob A; Gay I; Tsitsianov J; Shapiro T; Jatziv S; Ashkenazi A
Clin Genet; 1973; 4(3):275-8. PubMed ID: 4765211
[No Abstract] [Full Text] [Related]
5. Cochlear deafness, myopia, and intellectual impairment in an Amish family.
Eldridge R; Berlin CI; Money JW; McKusick VA
Arch Otolaryngol; 1968 Jul; 88(1):49-54. PubMed ID: 5660029
[No Abstract] [Full Text] [Related]
6. 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]
7. X-linked mental retardation, growth retardation, deafness and microgenitalism. A second familial report.
Mattei JF; Collignon P; Ayme S; Giraud F
Clin Genet; 1983 Jan; 23(1):70-4. PubMed ID: 6682021
[No Abstract] [Full Text] [Related]
8. 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]
9. 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]
10. Sex-linked congenital deafness.
McRae KN; Uchida IA; Lewis M
Am J Hum Genet; 1969 Sep; 21(5):415-22. PubMed ID: 5822288
[No Abstract] [Full Text] [Related]
11. A new case of DOOR syndrome.
Wiśniewska M; Siwińska Z; Felczak M; Wielkoszyński T; Krawczyński M; Latos-Bieleńska A
J Appl Genet; 2008; 49(1):101-3. PubMed ID: 18263975
[TBL] [Abstract][Full Text] [Related]
12. Wildervanck's syndrome. Hereditary malformations of the ear in three generations.
Shenoi PM
J Laryngol Otol; 1972 Nov; 86(11):1121-35. PubMed ID: 4636805
[No Abstract] [Full Text] [Related]
13. [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]
14. Acrocephalosyndactyly type 3: Chotzen's syndrome.
Bartsocas CS; Weber AL; Crawford JD
J Pediatr; 1970 Aug; 77(2):267-72. PubMed ID: 4393456
[No Abstract] [Full Text] [Related]
15. Otolaryngological disorders in craniometaphyseal dysplasia.
Kietzer G; Paparella MM
Laryngoscope; 1969 May; 79(5):921-41. PubMed ID: 5770043
[No Abstract] [Full Text] [Related]
16. Recessive microtia, meatal atresia, and hearing loss. Report of a sibship.
Konigsmark BW; Nager GT; Haskins HL
Arch Otolaryngol; 1972 Aug; 96(2):105-9. PubMed ID: 5081912
[No Abstract] [Full Text] [Related]
17. Audiometric identification of normal hearing carriers of genes for deafness.
Anderson H; Wedenberg E
Acta Otolaryngol; 1968 Jun; 65(6):535-54. PubMed ID: 5706025
[No Abstract] [Full Text] [Related]
18. 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]
19. Familial hand abnormality and sensori-neural deafness: a new syndrome.
Stewart JM; Bergstrom L
J Pediatr; 1971 Jan; 78(1):102-10. PubMed ID: 5539065
[No Abstract] [Full Text] [Related]
20. DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): elevated plasma and urinary 2-oxoglutarate in three unrelated patients.
Patton MA; Krywawych S; Winter RM; Brenton DP; Baraitser M
Am J Med Genet; 1987 Jan; 26(1):207-15. PubMed ID: 3812564
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]