Annals of the New York Academy of Sciences

Cover image for Annals of the New York Academy of Sciences

September 1991

Volume 630 Genetics of Hearing Impairment

Pages 1–321

    1. International Symposium on the Genetics of Hearing Impairment Introduction (pages 1–2)

      JAMES B. SNOW JR.

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19569.x

    2. Genetics of Hearing Impairment Welcome—an Overview (pages 3–5)

      SALOME G. WAELSCH

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19570.x

    3. The History of the Genetics of Hearing Impairment (pages 6–15)

      ROBERT J. RUBEN

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19571.x

    4. Genetic Epidemiology of Hearing Impairment (pages 16–31)

      N. E. MORTON

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19572.x

    5. The Genetic Anatomy of Hearing (pages 32–37)

      ROBERT W. MARION

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19573.x

    6. Human Genetic Mapping and Inherited Deafness Syndromes (pages 38–48)

      MARK F. LEPPERT and RICHARD A. LEWIS

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19574.x

    7. Comparative Gene Mapping, Genome Duplication, and the Genetics of Hearing (pages 49–67)

      JOSEPH H. NADEAU, MICHAEL KOSOWSKY and KAREN P. STEEL

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19575.x

    8. Reverse Genetics in the Mouse and Its Application to the Study of Deafness (pages 80–92)

      E. M. RINCHIK, D. K. JOHNSON, F. L. MARGOLIS, I J JACKSON, L. B. RUSSELL and D. A. CARPENTER

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19577.x

    9. Reverse Genetic Approaches to Cloning Deafness Genes (pages 93–99)

      S. D. M. BROWN, K. A. BROWN, M. J. SUTCLIFFE, J. S. CAVANNA, A. J. GREENFIELD and K. P. STEEL

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19578.x

  1. Genetic Analysis of Complex Disorders

    1. Top of page
    2. Genetic Analysis of Complex Disorders
    3. Neural Tube-Otic Anlage Interaction
    4. Medical and Cultural Considerations
    5. Poster Paper
    1. Genetic Analysis of Complex Disorders (pages 100–115)

      J. M. FRIEDMAN, R. L. LEIBEL, N. BAHARY, D. A. SIEGEL and G. TRUETT

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19579.x

  2. Neural Tube-Otic Anlage Interaction

    1. Top of page
    2. Genetic Analysis of Complex Disorders
    3. Neural Tube-Otic Anlage Interaction
    4. Medical and Cultural Considerations
    5. Poster Paper
    1. Gene Expression in Narmal and Abnormal Inner Ears (pages 129–132)

      ALLEN F. RYAN and and DONNA M. SIMMONS

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19581.x

    2. Localization of a Gene for Waardenburg Syndrome Type I (pages 143–151)

      ANDREW P. READ, CAROLE FOY, VALERIE NEWTON and RODNEY HARRIS

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19583.x

    3. Hearing Impairment and Pigmentary Disturbance (pages 152–166)

      PETER BEIGHTON, RAJKUMAR RAMESAR, INGRID WINSHIP, DENIS VILJOEN, JACQUIE GREENBERG, KAREN YOUNG, DIANA CURTIS and SEAN SELLARS

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19584.x

    4. Genetic Studies of Usher Syndrome (pages 167–175)

      W. J. KIMBERLING, M. D. WESTON, S. PIEKE DAHL, J. B. KENYON, Y. Y. SHUGART, C. MOLLER, S. L. H. DAVENPORT, A. MARTINI, M. MILANI and R. J. SMITH

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19585.x

    5. Molecular Genetics of X-Linked Hearing Impairment (pages 176–190)

      HAN G. BRUNNER, BERT SMEETS, DOMINIQUE SMEETS, MARCEL NELEN, COR W. R. J. CREMERS and HANS-HILGER ROPERS

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19586.x

    6. Nonsyndromal Profound Genetic Deafness in Childhood (pages 191–196)

      C. W. R. J. CREMERS, H. A. M. MARRES and P. M. van RIJN

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19587.x

    7. Acquired Causes of Deafness in Childhood (pages 197–202)

      COR W. R. J. CREMERS,

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19588.x

    8. Recurrence Risks (pages 203–211)

      SHELLEY D. SMITH

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19589.x

  3. Medical and Cultural Considerations

    1. Top of page
    2. Genetic Analysis of Complex Disorders
    3. Neural Tube-Otic Anlage Interaction
    4. Medical and Cultural Considerations
    5. Poster Paper
    1. Genetic Counseling of the Deaf (pages 212–222)

      KATHLEEN SHAVER ARNOS, JAMIE ISRAEL and MARGARET CUNNINGHAM

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19590.x

    1. Approaches to Genetic Counseling (pages 223–229)

      D. LINDHOUT, P. G. FRETS and M. F. NIERMEIJER

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19591.x

    2. Sociological Implications of Hearing Loss (pages 230–235)

      JOHN B. CHRISTIANSEN

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19592.x

    3. Ethical Issues in the Genetic Study of Deafness (pages 236–239)

      I. KING JORDAN

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19593.x

    4. Clinical and Genetic Aspects in Autosomal Dominant Inherited Osteogenesis Imperfecta Type I (pages 240–248)

      TON J. T. M. GARRETSEN and COR W. R. J. CREMERS

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19594.x

  4. Poster Paper

    1. Top of page
    2. Genetic Analysis of Complex Disorders
    3. Neural Tube-Otic Anlage Interaction
    4. Medical and Cultural Considerations
    5. Poster Paper
    1. An Evaluation of Otopathology in the MOV-13 Transgenic Mutant Mouse (pages 249–252)

      RICHARD A. ALTSCHULER, DAVID F. DOLAN, MARTIN PTOK, GANJEI GHOLIZADEH, JEFFREY BONADIO and JOSEPH E. HAWKINS

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19595.x

    2. Transforming Growth Factor-Beta : Paracrine Mediator of Otic Capsule Formation (pages 253–255)

      D. A. FRENZ, V. GALINOVIC-SCHWARTZ, H. STAECKER and T. R. VAN DE WATER

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19596.x

    3. Ultrastructural Changes of Cochlea in Mice with Hereditary Chondrodysplasia (cho/cho) (pages 259–261)

      H. CHO, Y. YAMADA and T. J. YOO

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19598.x

    4. The Molecular and Structural Basis of Hearing Impairment in Mice with the cpk Mutant Gene (pages 262–264)

      H. CHO, J. BUCHANAN, D. STRONG, Y. YAMADA and T. J. YOO

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19599.x

    5. Hearing Impairment in Mice with the cmd/cmd (Cartilage Matrix Deficiency) Mutant Gene (pages 265–267)

      T. J. YOO, H. CHO and Y. YAMADA

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19600.x

    6. Malformation and Degeneration Inner Ear of MOS Transgenic Mice (pages 268–269)

      STEVEN D. RAUCH and PAUL E. NEUMANN

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19601.x

    7. Neurosensory Relationships in the Cochlea of the Bronx Waltzer Mouse (pages 270–273)

      DONNA S. WHITLON and HANNA M. SOBKOWICZ

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19602.x

    8. Congenital Hypothyroidism : Vestibular and Auditory Damage in the Pigmented Rat (pages 274–276)

      G. MEZA, D. ACUÑA, Y. PEÑALOZA and A. POBLANO

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19603.x

    9. Anomalies of the Auditory Organ in Chromosomal Syndromes (pages 281–283)

      MITSUHITO SANO, MASAFUMI SAKAGAMI, TAMOTSU HARADA, TORU MATSUNAGA and MASAHIRO NAKAYAMA

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19605.x

    10. A Progress Report on the Localization of Usher Syndrome Type II to Chromosome 1q (pages 284–287)

      MICHAEL D. WESTON, WILLIAM J. KIMBERLING, CLAES G. MÖLLER, SANDRA PIEKE DAHL, RICHARD J. SMITH, ALESSANDRO MARTINI and MASSIMO MILANI

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19606.x

    11. The Search for Branchiootorenal Syndrome on Chromosomes 1 and 8 (pages 288–289)

      K. COMEAU, W. J. KIMBERLING, C. W. R. J. CREMERS and Y. SHUGART

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19607.x

    12. Profound Childhood Deafness in Southern Africa (pages 290–291)

      P. BEIGHTON, D. VILJOEN, I. WINSHIP, G. BEIGHTON and S. SELLARS

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19608.x

    13. National Deaf Register as a Resource for Hereditary Deafness Research (page 292)

      PAUL S. ING, BRENDA M. WERNIMONT, SHELLEY D. SMITH and WILLIAM J. KIMBERLING

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19609.x

    14. Ascertainment of Families with Hereditary Deafness for Linkage Studies (pages 293–294)

      C. STEVENS, K. ARNOS, J. BODURTHA, L. WRIGHT, B. RAWLINGS, M. MARAZITA, W. NANCE and S. DIEHL

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19610.x

    15. Report on Attempts to Localize Usher Syndrome Type 1 by Linkage Analysis to Selected Candidate Regions (pages 298–300)

      S. PIEKE DAHL, M. D. WESTON, W. J. KIMBERLING, J. B. KENYON, Y. Y. SHUGART and R. J. H. SMITH

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19612.x

    16. Mitochondrial Inheritance of Acquired Deafness (pages 301–302)

      M. GOLD, I. RAPIN and S. SHANSKE

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19613.x

    17. HLA Antigen Frequencies in Sensorineural Hearing Impairment of Suspected Genetic Origin (pages 303–304)

      M. MOURAD, M. TALAAT and M. ABOU KHATWA

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19614.x

    18. Neurofibromatosis 2 (Bilateral Acoustic or Central Neurofibromatosis), a Treatable Cause of Deafness (pages 305–307)

      D. M. PARRY, M. I. KAISER-KUPFER, J. L. SHERMAN, A. PIKUS and R. ELDRIDGE

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19615.x

    19. Assessment of Families from the Deaf Community (pages 308–309)

      JOHN T. ROLAND, ILENE D. MINER and NANCY SCULERATI

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19616.x

    20. Audiologic Profile in Niemann-Pick C (pages 313–314)

      ANITA PIKUS

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19618.x

    21. Hearing Loss Etiolgy in a group of 996 Children (pages 315–316)

      E. ARSLAN, P. TREVISI, E. GENOVESE, G. LUPI and S. PROSSER

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19619.x

    22. A Model Program for Genetic Counseling of the Deaf (pages 317–318)

      KATHLEEN SHAVER ARNOS, JAMIE ISRAEL and MARGARET CUNNINGHAM

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19620.x

    23. Otosderosis (pages 319–321)

      J. R. McPHEE, T. R. VAN DE WATER and M. A. GORDON

      Version of Record online: 17 DEC 2006 | DOI: 10.1111/j.1749-6632.1991.tb19621.x

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