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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

188 related items for PubMed ID: 6851230

  • 1. Autosomal dominant inheritance of conductive deafness due to stapedial anomalies, external ear malformations and congenital facial palsy.
    Sellars S, Beighton P.
    Clin Genet; 1983 May; 23(5):376-9. PubMed ID: 6851230
    [Abstract] [Full Text] [Related]

  • 2. An autosomal dominant inherited syndrome with congenital stapes ankylosis.
    Teunissen B, Cremers WR.
    Laryngoscope; 1990 Apr; 100(4):380-4. PubMed ID: 2319886
    [Abstract] [Full Text] [Related]

  • 3. Familial ossicular malformations: case report and review of literature.
    Higashi K, Yamakawa K, Itani O, Togawa K.
    Am J Med Genet; 1987 Nov; 28(3):655-9. PubMed ID: 3322009
    [Abstract] [Full Text] [Related]

  • 4. Congenital ossicular abnormalities: a review of 68 cases.
    Cousins VC, Milton CM.
    Am J Otol; 1988 Jan; 9(1):76-80. PubMed ID: 3364539
    [Abstract] [Full Text] [Related]

  • 5. Allograft stapes surgery for conductive hearing loss in patients with ossicular chain anomalies.
    Minatogawa T, Iritani H, Ishida K, Node MN.
    Eur Arch Otorhinolaryngol; 1996 Jan; 253(4-5):283-6. PubMed ID: 8737786
    [Abstract] [Full Text] [Related]

  • 6. Familial microtia, meatal atresia, and conductive deafness in three siblings.
    Schmid M, Schröder M, Langenbeck U.
    Am J Med Genet; 1985 Oct; 22(2):327-32. PubMed ID: 4050865
    [Abstract] [Full Text] [Related]

  • 7. Conductive hearing loss, middle ear ossicular anomalies, malformed thickened lop auricles, and micrognathia. A rare autosomal dominant congenital syndrome.
    Schweitzer VG, Kemink JL, Graham MD.
    Am J Otol; 1984 Jul; 5(5):387-91. PubMed ID: 6476090
    [Abstract] [Full Text] [Related]

  • 8. Congenital conductive or mixed deafness, preauricular sinus, external ear anomaly, and commissural lip pits: an autosomal dominant inherited syndrome.
    Marres HA, Cremers CW.
    Ann Otol Rhinol Laryngol; 1991 Nov; 100(11):928-32. PubMed ID: 1746829
    [Abstract] [Full Text] [Related]

  • 9. A syndrome with mixed deafness, Mozart ear, middle and inner ear dysplasias.
    García-Cruz D, Sanchez-Corona J, Ruenes R, Paniagua M, Ortega I, Cantú JM.
    J Laryngol Otol; 1980 Jul; 94(7):773-8. PubMed ID: 6968802
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Hemifacial microsomia, ipsilateral facial palsy, and malformed auricle in two families: an autosomal dominant malformation.
    Robinow M, Reynolds JF, FitzGerald J, Bryant JA.
    Am J Med Genet Suppl; 1986 Jul; 2():129-33. PubMed ID: 3146282
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Classification of congenital middle ear anomalies. Report on 144 ears.
    Teunissen EB, Cremers WR.
    Ann Otol Rhinol Laryngol; 1993 Aug; 102(8 Pt 1):606-12. PubMed ID: 8352484
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Microtia with meatal atresia and conductive deafness: mild and severe manifestations within the same sibship.
    Strisciuglio P, Ballabio A, Parenti G.
    J Med Genet; 1986 Oct; 23(5):459-60. PubMed ID: 3783624
    [Abstract] [Full Text] [Related]

  • 18. Congenital fixation of the head of the stapes in three family members.
    Wetmore SJ, Gross AF.
    Ear Nose Throat J; 2011 Aug; 90(8):360-6. PubMed ID: 21853440
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.