American Journal of Medical Genetics Part A

Cover image for American Journal of Medical Genetics Part A

1 August 2006

Volume 140A, Issue 15

Pages 1617–1710

  1. Research Articles

    1. Top of page
    2. Research Articles
    3. Clinical Reports
    4. Research Letters
    5. Research Reviews
    6. Book Reviews
    7. Correspondence
    8. Errata
    1. First report of prevalence of non-syndromic hereditary prosopagnosia (HPA) (pages 1617–1622)

      Ingo Kennerknecht, Thomas Grueter, Brigitte Welling, Sebastian Wentzek, Jürgen Horst, Steve Edwards and Martina Grueter

      Version of Record online: 30 JUN 2006 | DOI: 10.1002/ajmg.a.31343

    2. Growth hormone therapy and scoliosis in patients with Prader–Willi syndrome (pages 1623–1627)

      T. Nagai, K. Obata, T. Ogata, N. Murakami, Y. Katada, A. Yoshino, S. Sakazume, Y. Tomita, R. Sakuta and N. Niikawa

      Version of Record online: 12 JUN 2006 | DOI: 10.1002/ajmg.a.31295

    3. Pre- and postnatal findings in trisomy 17 mosaicism (pages 1628–1636)

      Barbara Utermann, Mariluce Riegel, Dru Leistritz, Thomas Karall, Josef Wisser, Lorraine Meisner, Christine Fauth, Rosa Baldinger, Julie Johnson, Martin Erdel, Malgorzata Taralczak, Richard M. Pauli, Alessandra Baumer, Albert Schinzel and Dieter Kotzot

      Version of Record online: 26 JUN 2006 | DOI: 10.1002/ajmg.a.31319

  2. Clinical Reports

    1. Top of page
    2. Research Articles
    3. Clinical Reports
    4. Research Letters
    5. Research Reviews
    6. Book Reviews
    7. Correspondence
    8. Errata
    1. Genetic disorders among Palestinian Arabs. 4: Genetic clinics in the community (pages 1644–1646)

      Joël Zlotogora, Saleh Barges, Bishara Bisharat and Stavit A. Shalev

      Version of Record online: 7 JUL 2006 | DOI: 10.1002/ajmg.a.31342

    2. Complete trisomy 17p syndrome in a girl with der(14)t(14;17)(p11.2;p11.2) (pages 1647–1654)

      Fady M. Mikhail, Dawn McIlvried, R. Lynn Holt, Ludwine Messiaen, Maria D. Descartes and Andrew J. Carroll

      Version of Record online: 11 JUL 2006 | DOI: 10.1002/ajmg.a.31330

    3. Opitz trigonocephaly C syndrome in a boy with a de novo balanced reciprocal translocation t(3;18)(q13.13;q12.1) (pages 1655–1657)

      Yasutsugu Chinen, Tadashi Kaname, Kumiko Yanagi, Nakamichi Saito, Kenji Naritomi and Takao Ohta

      Version of Record online: 11 JUL 2006 | DOI: 10.1002/ajmg.a.31341

    4. Trisomy 8q and partial trisomy 22 in a 43-year-old man with moderate intellectual disability, epilepsy and large cell non-Hodgkin lymphoma (pages 1658–1662)

      Ingo Helbig, Michael Wirtenberger, Anna Jauch, Hans-Dieter Hager, Gholamali Tariverdian, Kari Hemminki, Barbara Burwinkel and Ruediger Klaes

      Version of Record online: 12 JUL 2006 | DOI: 10.1002/ajmg.a.31350

    5. Extensive acrochordons and pancreatic islet-cell tumors in tuberous sclerosis associated with TSC2 mutations (pages 1669–1672)

      J. Lawrence Merritt II, Dawn Marie R. Davis, Mark R. Pittelkow and Dusica Babovic-Vuksanovic

      Version of Record online: 11 JUL 2006 | DOI: 10.1002/ajmg.a.31351

  3. Research Letters

    1. Top of page
    2. Research Articles
    3. Clinical Reports
    4. Research Letters
    5. Research Reviews
    6. Book Reviews
    7. Correspondence
    8. Errata
    1. Further cases of “neighbor” mutations in mucopolysaccharidosis type II (pages 1684–1686)

      Ida V. D. Schwartz, Luciane C. Lima, Karen Tylee, Ruy P. Oliveira Sobrinho, Denise Y. J. Norato, Andréa R. Duarte, Guy Besley, Maira G. Burin, Ursula Matte, Roberto Giugliani and Sandra Leistner-Segal

      Version of Record online: 12 JUN 2006 | DOI: 10.1002/ajmg.a.31317

    2. Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene (pages 1687–1691)

      Casey M. Rand, Debra E. Weese-Mayer, Lili Zhou, Brion S. Maher, Margaret E. Cooper, Mary L. Marazita and Elizabeth M. Berry-Kravis

      Version of Record online: 7 JUL 2006 | DOI: 10.1002/ajmg.a.31336

    3. Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia (pages 1692–1695)

      Jason Neal, Kira Apse, Mustafa Sahin, Christopher A. Walsh and Volney L. Sheen

      Version of Record online: 11 JUL 2006 | DOI: 10.1002/ajmg.a.31334

  4. Research Reviews

    1. Top of page
    2. Research Articles
    3. Clinical Reports
    4. Research Letters
    5. Research Reviews
    6. Book Reviews
    7. Correspondence
    8. Errata
    1. Mosaic ring 20 with no detectable deletion by FISH analysis: Characteristic seizure disorder and literature review (pages 1696–1706)

      Ying S. Zou, Daniel L. Van Dyke, Erik C. Thorland, Harinderpal S. Chhabra, Virginia V. Michels, Jeannette G. Keefe, Melanie A. Lega, Molly A. Feely, Timothy S. Uphoff and Syed M. Jalal

      Version of Record online: 11 JUL 2006 | DOI: 10.1002/ajmg.a.31332

  5. Book Reviews

    1. Top of page
    2. Research Articles
    3. Clinical Reports
    4. Research Letters
    5. Research Reviews
    6. Book Reviews
    7. Correspondence
    8. Errata
    1. Book review (pages 1707–1708)

      Ronald G. Davidson

      Version of Record online: 11 MAY 2006 | DOI: 10.1002/ajmg.a.31282

  6. Correspondence

    1. Top of page
    2. Research Articles
    3. Clinical Reports
    4. Research Letters
    5. Research Reviews
    6. Book Reviews
    7. Correspondence
    8. Errata
  7. Errata

    1. Top of page
    2. Research Articles
    3. Clinical Reports
    4. Research Letters
    5. Research Reviews
    6. Book Reviews
    7. Correspondence
    8. Errata
    1. You have free access to this content

SEARCH

SEARCH BY CITATION