American Journal of Medical Genetics Part A

Cover image for American Journal of Medical Genetics Part A

1 November 2006

Volume 140A, Issue 21

Pages 2257–2385

  1. Research Articles

    1. Top of page
    2. Research Articles
    3. Clinical Reports
    4. Research Letters
    5. Book Reviews
    6. Correspondence
    7. Invited Comments
    1. Head circumference and height in autism: A study by the collaborative program of excellence in autism (pages 2257–2274)

      Janet E. Lainhart, Erin D. Bigler, Maureen Bocian, Hilary Coon, Elena Dinh, Geraldine Dawson, Curtis K. Deutsch, Michelle Dunn, Annette Estes, Helen Tager-Flusberg, Susan Folstein, Susan Hepburn, Susan Hyman, William McMahon, Nancy Minshew, Jeff Munson, Kathy Osann, Sally Ozonoff, Patricia Rodier, Sally Rogers, Marian Sigman, M. Anne Spence, Christopher J. Stodgell and Fred Volkmar

      Version of Record online: 4 OCT 2006 | DOI: 10.1002/ajmg.a.31465

    2. ADHD symptoms in children with FXS (pages 2275–2288)

      Kelly Sullivan, Deborah Hatton, Julie Hammer, John Sideris, Stephen Hooper, Peter Ornstein and Donald Bailey Jr.

      Version of Record online: 4 OCT 2006 | DOI: 10.1002/ajmg.a.31388

    3. Trends and racial disparities in muscular dystrophy deaths in the United States, 1983–1998: An analysis of multiple cause mortality data (pages 2289–2297)

      Aileen Kenneson, Katherine Kolor, Quanhe Yang, Richard S. Olney, Sonja A. Rasmussen and J.M. Friedman

      Version of Record online: 4 OCT 2006 | DOI: 10.1002/ajmg.a.31437

    4. Associated malformations in congenital diaphragmatic hernia cases in the last 15 years in a tertiary referral institute (pages 2298–2304)

      Ágnes Harmath, Júlia Hajdú, Ákos Csaba, Erik Hauzman, Barbara Pete, Éva Görbe, Anna Beke and Zoltán Papp

      Version of Record online: 11 OCT 2006 | DOI: 10.1002/ajmg.a.31470

    5. Attitudes of genetic counselors towards expanding newborn screening and offering predictive genetic testing to children (pages 2312–2319)

      Susan Hiraki, Kelly E. Ormond, Katherine Kim and Lainie Friedman Ross

      Version of Record online: 11 OCT 2006 | DOI: 10.1002/ajmg.a.31485

  2. Clinical Reports

    1. Top of page
    2. Research Articles
    3. Clinical Reports
    4. Research Letters
    5. Book Reviews
    6. Correspondence
    7. Invited Comments
    1. Terminal 14q32.33 deletion: Genotype–phenotype correlation (pages 2324–2329)

      M-L. Maurin, S. Brisset, M. Le Lorc'h, V. Poncet, P. Trioche, A. Aboura, P. Labrune and G. Tachdjian

      Version of Record online: 4 OCT 2006 | DOI: 10.1002/ajmg.a.31438

    2. Recurrent pancreatitis in mitochondrial cytopathy (pages 2330–2335)

      François-Guillaume Debray, Eric Drouin, Denise Herzog, Anne Lortie, Marie Lambert, Laurent Garel, Grant. A. Mitchell and Jacques L. Michaud

      Version of Record online: 4 OCT 2006 | DOI: 10.1002/ajmg.a.31457

    3. Sensenbrenner syndrome: A new member of the hepatorenal fibrocystic family (pages 2336–2340)

      Marco Zaffanello, Francesca Diomedi-Camassei, Maria Luisa Melzi, Giuliano Torre, Francesco Callea and Francesco Emma

      Version of Record online: 4 OCT 2006 | DOI: 10.1002/ajmg.a.31464

    4. A case surviving for over a year of renal tubular dysgenesis with compound heterozygous angiotensinogen gene mutations (pages 2355–2360)

      Mitsugu Uematsu, Osamu Sakamoto, Toshiyuki Nishio, Toshihiro Ohura, Tadashi Matsuda, Tetsuji Inagaki, Takaaki Abe, Kunihiro Okamura, Yoshiaki Kondo and Shigeru Tsuchiya

      Version of Record online: 11 OCT 2006 | DOI: 10.1002/ajmg.a.31448

    5. Atypical cases of Angelman syndrome (pages 2361–2364)

      Amy Lawson-Yuen, Bai-Lin Wu, Va Lip, Trilochan Sahoo and Virginia Kimonis

      Version of Record online: 11 OCT 2006 | DOI: 10.1002/ajmg.a.31481

  3. Research Letters

    1. Top of page
    2. Research Articles
    3. Clinical Reports
    4. Research Letters
    5. Book Reviews
    6. Correspondence
    7. Invited Comments
    1. You have free access to this content
      Trisomy 18: Changes in sex ratio during intrauterine life (pages 2365–2367)

      Dunja Niedrist, Mariluce Riegel, Josef Achermann, Valentin Rousson and Albert Schinzel

      Version of Record online: 4 OCT 2006 | DOI: 10.1002/ajmg.a.31474

    2. Analysis of a Scottish founder effect narrows the TAPVR-1 gene interval to chromosome 4q12 (pages 2368–2373)

      Steven B. Bleyl, Lorenzo D. Botto, John C. Carey, Luciana T. Young, Michael J. Bamshad, Mark F. Leppert and Kenneth Ward

      Version of Record online: 11 OCT 2006 | DOI: 10.1002/ajmg.a.31471

    3. Association between the NAT1 1095C > A polymorphism and homocysteine concentration (pages 2374–2377)

      Anna Stanisławska-Sachadyn, Liselotte E. Jensen, Carmel Kealey, Jayne V. Woodside, Ian S. Young, John M. Scott, Liam Murray, Colin A. Boreham, Helene McNulty, J.J. Strain and Alexander S. Whitehead

      Version of Record online: 11 OCT 2006 | DOI: 10.1002/ajmg.a.31475

  4. Book Reviews

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

    1. Top of page
    2. Research Articles
    3. Clinical Reports
    4. Research Letters
    5. Book Reviews
    6. Correspondence
    7. Invited Comments
    1. Oculo-oto-facial dysplasia (OOFD) versus Burn–McKeown syndrome (pages 2381–2382)

      Dagmar Wieczorek and Gabriele Gillessen-Kaesbach

      Version of Record online: 4 OCT 2006 | DOI: 10.1002/ajmg.a.31478

  6. Invited Comments

    1. Top of page
    2. Research Articles
    3. Clinical Reports
    4. Research Letters
    5. Book Reviews
    6. Correspondence
    7. Invited Comments
    1. RE: Correspondence from Wieczorek & Gillessen-Kaesbach and Hing & Parisi (page 2385)

      John M. Opitz and John Burn

      Version of Record online: 4 OCT 2006 | DOI: 10.1002/ajmg.a.31476

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