American Journal of Medical Genetics Part A

Cover image for American Journal of Medical Genetics Part A

Special Issue: The Genetic Basis of Deafness

15 July 2007

Volume 143A, Issue 14

Pages 1531–1678

  1. Invited Comments

    1. Top of page
    2. Invited Comments
    3. Research Articles
    4. Genetic Drift
    5. New Syndrome
    6. Clinical Reports
    7. Research Letters
    8. Research Reviews
  2. Research Articles

    1. Top of page
    2. Invited Comments
    3. Research Articles
    4. Genetic Drift
    5. New Syndrome
    6. Clinical Reports
    7. Research Letters
    8. Research Reviews
    1. Assessing parental attitudes toward genetic testing for childhood hearing loss: Before and after genetic consultation (pages 1546–1553)

      Yuelin Li, Annie G. Steinberg, Lisa Bain, Dinah Yaeger, Ari Bieler, Rachel Ewing, Girija Kaimal and Ian Krantz

      Version of Record online: 31 MAY 2007 | DOI: 10.1002/ajmg.a.31730

    2. A case for genetics education: Collaborating with speech-language pathologists and audiologists (pages 1554–1559)

      Erin K. Harvey, Susan Stanton, Jennifer Garrett, J. Neils-Strunjas and Nancy Steinberg Warren

      Version of Record online: 31 MAY 2007 | DOI: 10.1002/ajmg.a.31743

    3. Additional clinical manifestations in children with sensorineural hearing loss and biallelic GJB2 mutations: Who should be offered GJB2 testing? (pages 1560–1566)

      Margaret A. Kenna, Heidi L. Rehm, Caroline D. Robson, Anna Frangulov, Jennifer McCallum, Dinah Yaeger and Ian D. Krantz

      Version of Record online: 23 APR 2007 | DOI: 10.1002/ajmg.a.31706

    4. Molecular genetics study of deafness in Brazil: 8-year experience (pages 1574–1579)

      Camila Andréa de Oliveira, Fabiana Alexandrino, Thalita Vitachi Christiani, Carlos Eduardo Steiner, José Luiz Rosemberis Cunha, Andréa Trevas Maciel Guerra and Edi Lúcia Sartorato

      Version of Record online: 13 JUN 2007 | DOI: 10.1002/ajmg.a.31838

    5. Molecular study in Brazilian cochlear implant recipients (pages 1580–1582)

      Thalita Vitachi Christiani, Fabiana Alexandrino, Camila Andréa de Oliveira, Regina Célia Bortoleto Amantini, Maria Cecília Bevilacqua, Orozimbo Alves Costa Filho, Paulo Porto and a. Edi Lúcia Sartorato

      Version of Record online: 13 JUN 2007 | DOI: 10.1002/ajmg.a.31778

    6. Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: Evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain (pages 1592–1598)

      Tomoko Makishima, Anne C. Madeo, Carmen C. Brewer, Christopher K. Zalewski, John A. Butman, Vandana Sachdev, Andrew E. Arai, Brenda M. Holbrook, Douglas R. Rosing and Andrew J. Griffith

      Version of Record online: 13 JUN 2007 | DOI: 10.1002/ajmg.a.31793

    7. A novel splice site mutation in EYA4 causes DFNA10 hearing loss (pages 1599–1604)

      Michael S. Hildebrand, David Coman, Tao Yang, R.J. McKinlay Gardner, Elizabeth Rose, Richard J.H. Smith, Melanie Bahlo and Hans-Henrik M. Dahl

      Version of Record online: 13 JUN 2007 | DOI: 10.1002/ajmg.a.31860

    8. Identification of novel mutations in WFS1 and genotype–phenotype correlation in Wolfram syndrome (pages 1605–1612)

      A. Cano, C. Rouzier, S. Monnot, B. Chabrol, J. Conrath, P. Lecomte, B. Delobel, P. Boileau, R. Valero, V. Procaccio, V. Paquis-Flucklinger and B. Vialettes

      Version of Record online: 13 JUN 2007 | DOI: 10.1002/ajmg.a.31809

    9. Phenotype description of a Dutch otosclerosis family with suggestive linkage to OTSC7 (pages 1613–1622)

      Robert Jan Pauw, Patrick L.M. Huygen, Melissa Thys, Guy Van Camp, Frank B.M. Joosten and Cor W.R.J. Cremers

      Version of Record online: 13 JUN 2007 | DOI: 10.1002/ajmg.a.31807

    10. Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus (pages 1623–1629)

      Nicole C. Meyer, Fatemeh Alasti, Carla J. Nishimura, Parisa Imanirad, Kimia Kahrizi, Yasser Riazalhosseini, Mahdi Malekpour, Nafiseh Kochakian, Payman Jamali, Guy Van Camp, Richard J.H. Smith and Hossein Najmabadi

      Version of Record online: 12 APR 2007 | DOI: 10.1002/ajmg.a.31718

    11. Methylthioadenosine phosphorylase (MTAP) in hearing: Gene disruption by chromosomal rearrangement in a hearing impaired individual and model organism analysis (pages 1630–1639)

      Robin E. Williamson, Keith N. Darrow, Sebastien Michaud, Julie S. Jacobs, Marilyn C. Jones, Daniel F. Eberl, Richard L. Maas, M. Charles Liberman and Cynthia C. Morton

      Version of Record online: 29 MAY 2007 | DOI: 10.1002/ajmg.a.31724

  3. Genetic Drift

    1. Top of page
    2. Invited Comments
    3. Research Articles
    4. Genetic Drift
    5. New Syndrome
    6. Clinical Reports
    7. Research Letters
    8. Research Reviews
    1. You have free access to this content
  4. New Syndrome

    1. Top of page
    2. Invited Comments
    3. Research Articles
    4. Genetic Drift
    5. New Syndrome
    6. Clinical Reports
    7. Research Letters
    8. Research Reviews
    1. You have free access to this content
  5. Clinical Reports

    1. Top of page
    2. Invited Comments
    3. Research Articles
    4. Genetic Drift
    5. New Syndrome
    6. Clinical Reports
    7. Research Letters
    8. Research Reviews
    1. Clinical and genetic analysis of two Tunisian otosclerosis families (pages 1653–1660)

      Insaf Bel Hadj Ali, Melissa Thys, Najeh Beltaief, Isabelle Schrauwen, Nele Dieltjens, Kathleen Vanderstraeten, Ghazi Besbes, Emna Mnif, Slah Hachicha, Saïda Ben Arab and Guy Van Camp

      Version of Record online: 13 JUN 2007 | DOI: 10.1002/ajmg.a.31806

    2. Familial unilateral deafness and delayed endolymphatic hydrops (pages 1661–1665)

      Kelley M. Dodson, Tamio Kamei, Aristides Sismanis and Walter E. Nance

      Version of Record online: 11 MAY 2007 | DOI: 10.1002/ajmg.a.31741

  6. Research Letters

    1. Top of page
    2. Invited Comments
    3. Research Articles
    4. Genetic Drift
    5. New Syndrome
    6. Clinical Reports
    7. Research Letters
    8. Research Reviews
    1. Epidemiological study of nonsyndromic hearing loss in Sicilian newborns (pages 1666–1670)

      M. Niceta, C. Fabiano, P. Sammarco, M. Piccione, V. Antona, M. Giuffrè and G. Corsello

      Version of Record online: 13 JUN 2007 | DOI: 10.1002/ajmg.a.31836

  7. Research Reviews

    1. Top of page
    2. Invited Comments
    3. Research Articles
    4. Genetic Drift
    5. New Syndrome
    6. Clinical Reports
    7. Research Letters
    8. Research Reviews
    1. Branchio-oto-renal syndrome (pages 1671–1678)

      Amit Kochhar, Stephanie M. Fischer, William J. Kimberling and Richard J.H. Smith

      Version of Record online: 19 JAN 2007 | DOI: 10.1002/ajmg.a.31561

SEARCH

SEARCH BY CITATION