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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

127 related items for PubMed ID: 6717641

  • 1. [Stapes ankylosis as a symptom of autosomal dominant symphalangia].
    Theunissen EJ, Cremers CW.
    Ned Tijdschr Geneeskd; 1984 Apr 14; 128(15):712-4. PubMed ID: 6717641
    [No Abstract] [Full Text] [Related]

  • 2. Proximal symphalangia and stapes ankylosis.
    Cremers C, Theunissen E, Kuijpers W.
    Arch Otolaryngol; 1985 Nov 14; 111(11):765-7. PubMed ID: 4051868
    [Abstract] [Full Text] [Related]

  • 3. An autosomal dominant inherited syndrome with congenital stapes ankylosis.
    Teunissen B, Cremers WR.
    Laryngoscope; 1990 Apr 14; 100(4):380-4. PubMed ID: 2319886
    [Abstract] [Full Text] [Related]

  • 4. Congenital stapes fixation, symphalangism and syndactylia.
    Vase P, Prytz S, Pedersen PS.
    Acta Otolaryngol; 1975 Apr 14; 80(5-6):394-8. PubMed ID: 173134
    [Abstract] [Full Text] [Related]

  • 5. [Hand and foot deformities in a type I trichorhinophalangeal syndrome. Studies in 3 members of a family].
    Meyer HH, Prescher W, Reime J.
    Z Orthop Ihre Grenzgeb; 1988 Apr 14; 126(1):34-8. PubMed ID: 3381568
    [Abstract] [Full Text] [Related]

  • 6. [Symphalangisms and stapes ankylosis].
    Stenger HH, Gloede JF.
    Arch Klin Exp Ohren Nasen Kehlkopfheilkd; 1972 Apr 14; 202(2):632-4. PubMed ID: 4646150
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. [Transverse extremity defects in a case of Adams-Oliver syndrome].
    Fehlow P, Walther F.
    Padiatr Grenzgeb; 1990 Apr 14; 29(4):279-84. PubMed ID: 2216522
    [Abstract] [Full Text] [Related]

  • 9. Dominant symphalangism and conductive hearing loss.
    Makowski A, Latkowski B, Niebudek-Bogusz E.
    Rev Laryngol Otol Rhinol (Bord); 1995 Apr 14; 116(5):339-40. PubMed ID: 8677370
    [Abstract] [Full Text] [Related]

  • 10. [Syndrome of symphalangism and stapes fixation: an autosomal dominant hereditary disease (author's transl)].
    Meinecke P, Passarge E.
    Dtsch Med Wochenschr; 1978 Oct 20; 103(42):1660, 1663-5. PubMed ID: 699789
    [Abstract] [Full Text] [Related]

  • 11. Otosclerosis or congenital stapes ankylosis? The diagnostic role of genetic analysis.
    Emery SB, Meyer A, Miller L, Lesperance MM.
    Otol Neurotol; 2009 Dec 20; 30(8):1204-8. PubMed ID: 19471170
    [Abstract] [Full Text] [Related]

  • 12. Craniosynostosis, Philadelphia type: a new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toes.
    Robin NH, Segel B, Carpenter G, Muenke M.
    Am J Med Genet; 1996 Mar 15; 62(2):184-91. PubMed ID: 8882401
    [Abstract] [Full Text] [Related]

  • 13. Characterization of a stapes ankylosis family with a NOG mutation.
    Brown DJ, Kim TB, Petty EM, Downs CA, Martin DM, Strouse PJ, Moroi SE, Gebarski SS, Lesperance MM.
    Otol Neurotol; 2003 Mar 15; 24(2):210-5. PubMed ID: 12621334
    [Abstract] [Full Text] [Related]

  • 14. [Holt syndrome: an autosomal dominant, heterogeneous, acral malformation].
    Hernández Téllez A, Corona Rivera E, Martínez-Basalo C, Nazará Cazorla Z, Aguirre-Negrete MG, Cantú JM.
    Bol Med Hosp Infant Mex; 1982 Feb 15; 39(2):131-3. PubMed ID: 7093017
    [No Abstract] [Full Text] [Related]

  • 15. [Hereditary type E brachydactylia. Apropos of a familial case].
    Gnamey D, Walbaum R, Fossati P, Prouvost JM.
    Pediatrie; 1975 Mar 15; 30(2):153-9. PubMed ID: 165459
    [No Abstract] [Full Text] [Related]

  • 16. [Polydactyly].
    Le Marec B, Bracq H, Lambotte C, Nivelon A, Pfeiffer R, Toudic L.
    J Genet Hum; 1982 Nov 15; 30(4):317-28. PubMed ID: 7169597
    [Abstract] [Full Text] [Related]

  • 17. Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin.
    Brown DJ, Kim TB, Petty EM, Downs CA, Martin DM, Strouse PJ, Moroi SE, Milunsky JM, Lesperance MM.
    Am J Hum Genet; 2002 Sep 15; 71(3):618-24. PubMed ID: 12089654
    [Abstract] [Full Text] [Related]

  • 18. [Hereditary brachydactyly with nail aplasia].
    Santos HG, George FH, Ferreira JR.
    Acta Med Port; 1981 Sep 15; 3(2):147-60. PubMed ID: 7315521
    [No Abstract] [Full Text] [Related]

  • 19. [Stapes fixation and proximal symphalangism caused by autosomal dominant transmission (author's transl)].
    Baschek V.
    Laryngol Rhinol Otol (Stuttg); 1978 Apr 15; 57(4):299-304. PubMed ID: 651475
    [Abstract] [Full Text] [Related]

  • 20. [Genetic morphological fatal syndrome. Smith-Lemli-Opitz syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Mar 15; 14(2):91-2. PubMed ID: 8469651
    [No Abstract] [Full Text] [Related]

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