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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

163 related items for PubMed ID: 2904400

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  • 2. X-linked mixed deafness with stapes fixation in a Mauritian kindred: linkage to Xq probe pDP34.
    Wallis C, Ballo R, Wallis G, Beighton P, Goldblatt J.
    Genomics; 1988 Nov; 3(4):299-301. PubMed ID: 3243543
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  • 4. Clinical features of female heterozygotes in the X-linked mixed deafness syndrome (with perilymphatic gusher during stapes surgery).
    Cremers CW, Huygen PL.
    Int J Pediatr Otorhinolaryngol; 1983 Nov; 6(2):179-85. PubMed ID: 6662621
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  • 5. Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21.
    Merry DE, Lesko JG, Sosnoski DM, Lewis RA, Lubinsky M, Trask B, van den Engh G, Collins FS, Nussbaum RL.
    Am J Hum Genet; 1989 Oct; 45(4):530-40. PubMed ID: 2491012
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  • 9. 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
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  • 15. Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4.
    de Kok YJ, van der Maarel SM, Bitner-Glindzicz M, Huber I, Monaco AP, Malcolm S, Pembrey ME, Ropers HH, Cremers FP.
    Science; 1995 Feb 03; 267(5198):685-8. PubMed ID: 7839145
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  • 16. X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21.
    Piussan C, Hanauer A, Dahl N, Mathieu M, Kolski C, Biancalana V, Heyberger S, Strunski V.
    Am J Hum Genet; 1995 Jan 03; 56(1):224-30. PubMed ID: 7825582
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  • 18. [Congenital cerebrospinal fluid pressure labyrinth].
    Michel O, Breunsbach J, Matthias R.
    HNO; 1991 Dec 03; 39(12):486-90. PubMed ID: 1794964
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