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There are 8174 results for: content related to: Experience with hemihyperplasia and Beckwith–Wiedemann syndrome surveillance protocol

  1. Risk of tumorigenesis in overgrowth syndromes: A comprehensive review

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 137C, Issue 1, 15 August 2005, Pages: 53–71, Pablo Lapunzina

    Article first published online : 11 JUL 2005, DOI: 10.1002/ajmg.c.30064

  2. Beckwith–Wiedemann syndrome

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 137C, Issue 1, 15 August 2005, Pages: 12–23, Rosanna Weksberg, Cheryl Shuman and Adam C. Smith

    Article first published online : 11 JUL 2005, DOI: 10.1002/ajmg.c.30058

  3. You have free access to this content
    Bilateral Pheochromocytomas, Hemihyperplasia, and Subtle Somatic Mosaicism: The Importance of Detecting Low-Level Uniparental Disomy

    American Journal of Medical Genetics Part A

    Volume 161, Issue 5, May 2013, Pages: 993–1001, Jennifer M. Kalish, Laura K. Conlin, Sogol Mostoufi-Moab, Alisha B. Wilkens, Surabhi Mulchandani, Kristin Zelley, Megan Kowalski, Tricia R. Bhatti, Pierre Russo, Peter Mattei, William G. Mackenzie, Virginia LiVolsi, Kim E. Nichols, Jaclyn A. Biegel, Nancy B. Spinner and Matthew A. Deardorff

    Article first published online : 26 MAR 2013, DOI: 10.1002/ajmg.a.35831

  4. Severe presentation of Beckwith–Wiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 24, 15 December 2007, Pages: 3010–3015, Adam C. Smith, Cheryl Shuman, David Chitayat, Leslie Steele, Peter N. Ray, Jaqueline Bourgeois and Rosanna Weksberg

    Article first published online : 13 NOV 2007, DOI: 10.1002/ajmg.a.32030

  5. Tumor risk in Beckwith–Wiedemann syndrome: A review and meta-analysis

    American Journal of Medical Genetics Part A

    Volume 136A, Issue 1, 1 July 2005, Pages: 95–104, P. Rump, M.P.A. Zeegers and A.J. van Essen

    Article first published online : 10 MAY 2005, DOI: 10.1002/ajmg.a.30729

  6. Beckwith–Wiedemann syndrome

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 154C, Issue 3, 15 August 2010, Pages: 343–354, Sanaa Choufani, Cheryl Shuman and Rosanna Weksberg

    Article first published online : 20 AUG 2010, DOI: 10.1002/ajmg.c.30267

  7. You have free access to this content
    Tumour surveillance in Beckwith–Wiedemann syndrome and hemihyperplasia: A critical review of the evidence and suggested guidelines for local practice

    Journal of Paediatrics and Child Health

    Volume 42, Issue 9, September 2006, Pages: 486–490, Tiong Y Tan and David J Amor

    Article first published online : 18 AUG 2006, DOI: 10.1111/j.1440-1754.2006.00908.x

  8. Constitutional UPD for chromosome 11p15 in individuals with isolated hemihyperplasia is associated with high tumor risk and occurs following assisted reproductive technologies

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 14, 15 July 2006, Pages: 1497–1503, Cheryl Shuman, Adam C. Smith, Leslie Steele, Peter N. Ray, Carol Clericuzio, Elaine Zackai, Melissa A. Parisi, Anna T. Meadows, Thaddeus Kelly, David Tichauer, Jeremy A. Squire, Paul Sadowski and Rosanna Weksberg

    Article first published online : 12 JUN 2006, DOI: 10.1002/ajmg.a.31323

  9. Brain abnormalities in patients with Beckwith–Wiedemann syndrome

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 6, June 2012, Pages: 1388–1394, Kate Gardiner, David Chitayat, Sanaa Choufani, Cheryl Shuman, Susan Blaser, Deborah Terespolsky, Sandra Farrell, Rosemary Reiss, Shoshana Wodak, Shuye Pu, Peter N. Ray, Berivan Baskin and Rosanna Weksberg

    Article first published online : 14 MAY 2012, DOI: 10.1002/ajmg.a.35358

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    Clinical features of three girls with mosaic genome-wide paternal uniparental isodisomy

    American Journal of Medical Genetics Part A

    Volume 161, Issue 8, August 2013, Pages: 1929–1939, Jennifer M. Kalish, Laura K. Conlin, Tricia R. Bhatti, Holly A. Dubbs, Mary Catherine Harris, Kosuke Izumi, Sogol Mostoufi-Moab, Surabhi Mulchandani, Sulagna Saitta, Lisa J. States, Daniel T. Swarr, Alisha B. Wilkens, Elaine H. Zackai, Kristin Zelley, Marisa S. Bartolomei, Kim E. Nichols, Andrew A. Palladino, Nancy B. Spinner and Matthew A. Deardorff

    Article first published online : 26 JUN 2013, DOI: 10.1002/ajmg.a.36045

  11. The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: Two new reports

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 2, 15 January 2008, Pages: 137–148, Meredith Wilson, Gregory Peters, Bruce Bennetts, George McGillivray, Zan He Wu, Christopher Poon and Elizabeth Algar

    Article first published online : 21 NOV 2007, DOI: 10.1002/ajmg.a.32172

  12. Molecular Findings in Beckwith–Wiedemann Syndrome

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 163, Issue 2, May 2013, Pages: 131–140, SANAA CHOUFANI, CHERYL SHUMAN and ROSANNA WEKSBERG

    Article first published online : 16 APR 2013, DOI: 10.1002/ajmg.c.31363

  13. Fibroadenoma in Beckwith–Wiedemann syndrome with paternal uniparental disomy of chromosome 11p15.5

    Pediatrics International

    Volume 56, Issue 6, December 2014, Pages: 931–934, Yuichi Takama, Akio Kubota, Masahiro Nakayama, Ken Higashimoto, Kosuke Jozaki and Hidenobu Soejima

    Article first published online : 18 DEC 2014, DOI: 10.1111/ped.12406

  14. Recognition and management of childhood cancer syndromes: A systems approach

    American Journal of Medical Genetics

    Volume 89, Issue 2, 25 June 1999, Pages: 81–90, Carol L. Clericuzio

    Article first published online : 11 NOV 1999, DOI: 10.1002/(SICI)1096-8628(19990625)89:2<81::AID-AJMG5>3.0.CO;2-I

  15. DNA methylation studies on imprinted loci in a male monozygotic twin pair discordant for Beckwith–Wiedemann syndrome

    Clinical Genetics

    Volume 79, Issue 6, June 2011, Pages: 546–553, S Tierling, NY Souren, S Reither, KD Zang, J Meng-Hentschel, D Leitner, B Oehl-Jaschkowitz and J Walter

    Article first published online : 7 JUN 2010, DOI: 10.1111/j.1399-0004.2010.01482.x

  16. You have free access to this content
    In this issue

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 6, June 2010, Page: fm x,

    Article first published online : 20 MAY 2010, DOI: 10.1002/ajmg.a.33536

  17. Presence of Vascular Anomalies with Congenital Hemihypertrophy and Wilms Tumor: An Evidence-Based Evaluation

    Pediatric Dermatology

    Volume 20, Issue 3, May 2003, Pages: 199–206, Roopal V. Kundu and Ilona J. Frieden

    Article first published online : 28 MAY 2003, DOI: 10.1046/j.1525-1470.2003.20303.x

  18. Poikiloderma with Neutropenia: Report of Three Cases Including One with Calcinosis Cutis

    Pediatric Dermatology

    Volume 29, Issue 4, July/August 2012, Pages: 463–472, Rattanavalai Chantorn and Tor Shwayder

    Article first published online : 4 OCT 2011, DOI: 10.1111/j.1525-1470.2011.01513.x

  19. Genetics of Beckwith-Wiedemann syndrome-associated tumors: Common genetic pathways

    Genes, Chromosomes and Cancer

    Volume 28, Issue 1, May 2000, Pages: 1–13, Marja Steenman, Andries Westerveld and Marcel Mannens

    Article first published online : 28 MAR 2000, DOI: 10.1002/(SICI)1098-2264(200005)28:1<1::AID-GCC1>3.0.CO;2-#

  20. 44th Congress of the International Society of Paediatric Oncology (SIOP) 2012, London, United Kingdom, 5th–8th October, 2012 SIOP abstracts

    Pediatric Blood & Cancer

    Volume 59, Issue 6, 1 December 2012, Pages: 965–1152,

    Article first published online : 17 SEP 2012, DOI: 10.1002/pbc.24295