Search Results

There are 3944985 results for: content related to: Special section. Syndrome-specific growth charts

  1. You have free access to this content
    Growth curves of Egyptian patients with Turner syndrome

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: 2687–2691, Hala T. El-Bassyouni, Hanan H. Afifi, Mona S. Aglan, Wael M. Mahmoud and Moushira E. Zaki

    Version of Record online : 27 JUL 2012, DOI: 10.1002/ajmg.a.35518

  2. You have free access to this content
    Table of Contents, Volume 158A, Number 11, November 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: fm i–fm vi,

    Version of Record online : 18 OCT 2012, DOI: 10.1002/ajmg.a.35745

  3. You have free access to this content
    Development and implementation of electronic growth charts for infants with Prader–Willi syndrome

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: 2743–2749, S. Trent Rosenbloom and Merlin G. Butler

    Version of Record online : 17 AUG 2012, DOI: 10.1002/ajmg.a.35581

  4. You have free access to this content
    Growth charts of Down syndrome in Egypt: A study of 434 children 0–36 months of age

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: 2647–2655, Hanan H. Afifi, Mona S. Aglan, Moushira E. Zaki, Manal M. Thomas and Angie M.S. Tosson

    Version of Record online : 18 JUL 2012, DOI: 10.1002/ajmg.a.35468

  5. Weaver syndrome and defective cortical development: A rare association

    American Journal of Medical Genetics Part A

    Volume 161, Issue 1, January 2013, Pages: 225–227, Ahmed Al-Salem, Muneera J. Alshammari, Hamdy Hassan, Anas M. Alazami and Fowzan S. Alkuraya

    Version of Record online : 13 DEC 2012, DOI: 10.1002/ajmg.a.35660

  6. Recurrence of osteogenesis imperfecta due to maternal mosaicism of a novel COL1A1 mutation

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: 2969–2971, Takahiro Yamada, Masaki Takagi, Gen Nishimura, Rina Akaishi, Itsuko Furuta, Mamoru Morikawa, Takashi Yamada, Kazutoshi Cho, Hideaki Sawai, Shiro Ikegawa, Tomonobu Hasegawa and Hisanori Minakami

    Version of Record online : 17 SEP 2012, DOI: 10.1002/ajmg.a.35602

  7. You have free access to this content
    American Journal of Medical Genetics Part A: Volume 158A, Number 6, June 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 6, June 2012, Page: C1,

    Version of Record online : 17 MAY 2012, DOI: 10.1002/ajmg.a.35510

  8. Increased risk of breast cancer in women with NF1

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 12, December 2012, Pages: 3056–3060, Sara Aileen Madanikia, Amanda Bergner, Xiaobu Ye and Jaishri O'Neill Blakeley

    Version of Record online : 19 NOV 2012, DOI: 10.1002/ajmg.a.35550

  9. Clinical expression in Pfeiffer syndrome type 2 and 3: Surveillance in Japan

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 10, October 2012, Pages: 2506–2510, Hiroshi Koga, Naohiro Suga, Takato Nakamoto, Koichi Tanaka and Noboru Takahashi

    Version of Record online : 10 SEP 2012, DOI: 10.1002/ajmg.a.35590

  10. The signature of craniofacial deformation in fibrodysplasia ossificans progressiva

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: 2977–2978, Daniel Rocha Carvalho, Luciano Farage and Carlos Eduardo Speck-Martins

    Version of Record online : 17 SEP 2012, DOI: 10.1002/ajmg.a.35617

  11. You have free access to this content
    American Journal of Medical Genetics Part A: Volume 158A, Number 7, July 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 7, July 2012, Page: C1,

    Version of Record online : 18 JUN 2012, DOI: 10.1002/ajmg.a.35543

  12. Hyperinsulinemic hypoglycemia of infancy in Sotos syndrome

    American Journal of Medical Genetics Part A

    Volume 161, Issue 1, January 2013, Pages: 34–37, Terumichi Matsuo, Dr. Kenji Ihara, Masayuki Ochiai, Tadamune Kinjo, Yoko Yoshikawa, Kanako Kojima-Ishii, Marie Noda, Hiroshi Mizumoto, Maiko Misaki, Kyoko Minagawa, Koji Tominaga and Toshiro Hara

    Version of Record online : 13 DEC 2012, DOI: 10.1002/ajmg.a.35657

  13. Severe lateral tibial bowing with short stature in two siblings—A provisionally novel syndrome

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 9, September 2012, Pages: 2309–2316, Lia Zitano, Randall T. Loder, Mervyn D. Cohen and David D. Weaver

    Version of Record online : 1 AUG 2012, DOI: 10.1002/ajmg.a.35514

  14. Sleep-disordered breathing in Beckwith–Wiedemann syndrome: Three patients

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: 2956–2958, Sujay Kansagra, O'Neill D'Cruz, Terry L. Noah and Bradley V. Vaughn

    Version of Record online : 14 SEP 2012, DOI: 10.1002/ajmg.a.35628

  15. Sirenomelia and cyclopia in the same patient after a cluster of cyclopia and sirenomelia in Cali (South America)

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 7, July 2012, Pages: 1808–1810, Harry Pachajoa and Carolina Isaza

    Version of Record online : 24 MAY 2012, DOI: 10.1002/ajmg.a.35411

  16. You have free access to this content
    American Journal of Medical Genetics Part A: Volume 158A, Number 5, May 2012

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 5, May 2012, Page: C1,

    Version of Record online : 19 APR 2012, DOI: 10.1002/ajmg.a.35451

  17. Medical complications, clinical findings, and educational outcomes in adults with Noonan syndrome

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 12, December 2012, Pages: 3106–3111, Patroula Smpokou, Erica Tworog-Dube, Raju S. Kucherlapati and Amy E. Roberts

    Version of Record online : 19 NOV 2012, DOI: 10.1002/ajmg.a.35639

  18. Severe craniosynostosis in an infant with deletion 22q11.2 syndrome

    American Journal of Medical Genetics Part A

    Volume 161, Issue 1, January 2013, Pages: 153–157, W. Al-Hertani, V.A. Hastings, J. McGowan-Jordan, J. Hurteau and Gail E. Graham

    Version of Record online : 13 DEC 2012, DOI: 10.1002/ajmg.a.35491

  19. Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 7, July 2012, Pages: 1750–1753, Piranit Nik Kantaputra, Ans van den Ouweland, Tumtip Sangruchi and Chanin Limwongse

    Version of Record online : 7 JUN 2012, DOI: 10.1002/ajmg.a.35422

  20. Is monosomy 21 rare? Seven early miscarriages including one mosaic 45,XX,-21/44,X,-21 in a single study population

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 8, August 2012, Pages: 2050–2052, Philip Hardy, Jennifer Bryan, Roderick Hardy, Patrick A. Lennon and Kathy Hardy

    Version of Record online : 29 JUN 2012, DOI: 10.1002/ajmg.a.35462