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There are 3001 results for: content related to: Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: Modification of the Wolf–Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith–Wiedemann or Russell–Silver phenotype

  1. Overlapping phenotype of Wolf–Hirschhorn and Beckwith–Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter)

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 15, 1 August 2007, Pages: 1760–1766, Fady M. Mikhail, Achara Sathienkijkanchai, Nathaniel H. Robin, Sandra Prucka, Julie Sanford Biggerstaff, Jan Komorowski, Robin Andersson, Carl E.G. Bruder, Arkadiusz Piotrowski, Teresita Diaz de Ståhl, Jan P. Dumanski and Andrew J. Carroll

    Version of Record online : 29 JUN 2007, DOI: 10.1002/ajmg.a.31821

  2. 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

    Version of Record online : 20 AUG 2010, DOI: 10.1002/ajmg.c.30267

  3. You have free access to this content
    Clinical and molecular analyses of Beckwith–Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniques

    American Journal of Medical Genetics Part A

    Volume 170, Issue 10, October 2016, Pages: 2740–2749, Jair Tenorio, Valeria Romanelli, Alex Martin-Trujillo, García-Moya Fernández, Mabel Segovia, Claudia Perandones, Luis A. Pérez Jurado, Manel Esteller, Mario Fraga, Pedro Arias, Gema Gordo, Irene Dapía, Rocío Mena, María Palomares, Guiomar Pérez de Nanclares, Julián Nevado, Sixto García-Miñaur, Fernando Santos-Simarro, Víctor Martinez-Glez, Elena Vallespín, The SOGRI Consortium, David Monk and Pablo Lapunzina

    Version of Record online : 2 AUG 2016, DOI: 10.1002/ajmg.a.37852

  4. Undermining Reasonableness: Expert Testimony in a Case Involving a Battered Woman Who Kills

    Psychology of Women Quarterly

    Volume 27, Issue 1, March 2003, Pages: 37–45, Cheryl Terrance and Kimberly Matheson

    Version of Record online : 31 JAN 2003, DOI: 10.1111/1471-6402.t01-2-00005

  5. 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

    Version of Record online : 11 JUL 2005, DOI: 10.1002/ajmg.c.30058

  6. Isolated fetal omphalocele, Beckwith-Wiedemann syndrome, and assisted reproductive technologies

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 85, Issue 1, January 2009, Pages: 58–62, Louise Wilkins-Haug, Amina Porter, Pam Hawley and Carol B. Benson

    Version of Record online : 23 DEC 2008, DOI: 10.1002/bdra.20547

  7. Multiple hemangiomas in a patient with a t(3q;4p) translocation: An infrequent association with Wolf–Hirschhorn syndrome

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 2, 15 January 2008, Pages: 219–224, Sherly Pardo, Netta Blitman, Bokyung Han, Ninette Cohen, Lisa Edelmann and Kurt Hirschhorn

    Version of Record online : 12 DEC 2007, DOI: 10.1002/ajmg.a.32033

  8. Comparison of best–worst and hedonic scaling for the measurement of consumer wine preferences

    Australian Journal of Grape and Wine Research

    Volume 15, Issue 3, October 2009, Pages: 205–215, S. MUELLER, I.L. FRANCIS and L. LOCKSHIN

    Version of Record online : 5 MAR 2009, DOI: 10.1111/j.1755-0238.2009.00049.x

  9. Factors associated with preterm delivery in mothers of children with Beckwith–Wiedemann syndrome: A case cohort study from the BWS registry

    American Journal of Medical Genetics Part A

    Volume 134A, Issue 2, 15 April 2005, Pages: 187–191, Michael F. Wangler, Aimee S. Chang, Kelle H. Moley, Andrew P. Feinberg and Michael R. DeBaun

    Version of Record online : 18 FEB 2005, DOI: 10.1002/ajmg.a.30595

  10. Beckwith–Wiedemann syndrome

    Standard Article

    Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics

    Benjamin Tycko and Marcel Mannens

    Published Online : 15 NOV 2005, DOI: 10.1002/047001153X.g103213

  11. Epigenetic and genetic disturbance of the imprinted 11p15 region in Beckwith–Wiedemann and Silver–Russell syndromes

    Clinical Genetics

    Volume 81, Issue 4, April 2012, Pages: 350–361, J Demars and C Gicquel

    Version of Record online : 16 JAN 2012, DOI: 10.1111/j.1399-0004.2011.01822.x

  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

    Version of Record online : 16 APR 2013, DOI: 10.1002/ajmg.c.31363

  13. (Epi)genotype–phenotype correlations in Beckwith–Wiedemann syndrome: a paradigm for genomic medicine

    Clinical Genetics

    Volume 89, Issue 4, April 2016, Pages: 403–415, A. Mussa, S. Russo, L. Larizza, A. Riccio and G.B. Ferrero

    Version of Record online : 30 JUL 2015, DOI: 10.1111/cge.12635

  14. Phenotype, cancer risk, and surveillance in Beckwith–Wiedemann syndrome depending on molecular genetic subgroups

    American Journal of Medical Genetics Part A

    Volume 170, Issue 9, September 2016, Pages: 2248–2260, Saskia M. Maas, Fleur Vansenne, Daniel J. M. Kadouch, Abdulla Ibrahim, Jet Bliek, Saskia Hopman, Marcel M. Mannens, Johannes H. M. Merks, Eamonn R. Maher and Raoul C. Hennekam

    Version of Record online : 15 JUL 2016, DOI: 10.1002/ajmg.a.37801

  15. Beckwith–Wiedemann syndrome in sibs discordant for IC2 methylation

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 7, July 2012, Pages: 1662–1669, Karen Y. Niederhoffer, Maria Peñaherrera, Denise Pugash, Rosemarie Rupps, Laura Arbour, Francine Tessier, Sanaa Choufani, Chunhua Zhao, Irina Manokhina, Cheryl Shuman, Wendy P. Robinson, Rosanna Weksberg and Cornelius F. Boerkoel

    Version of Record online : 21 MAY 2012, DOI: 10.1002/ajmg.a.35377

  16. New insights into the pathogenesis of beckwith–wiedemann and silver–russell syndromes: Contribution of small copy number variations to 11p15 imprinting defects

    Human Mutation

    Volume 32, Issue 10, October 2011, Pages: 1171–1182, Julie Demars, Sylvie Rossignol, Irène Netchine, Kai Syin Lee, Mansur Shmela, Laurence Faivre, Jacques Weill, Sylvie Odent, Salah Azzi, Patrick Callier, Josette Lucas, Christèle Dubourg, Joris Andrieux, Yves Le Bouc, Assam El-Osta and Christine Gicquel

    Version of Record online : 8 SEP 2011, DOI: 10.1002/humu.21558

  17. You have free access to this content
    Interannual variability of the oceanic CO2 sink in the subtropical gyre of the North Atlantic Ocean over the last 2 decades

    Journal of Geophysical Research: Oceans (1978–2012)

    Volume 112, Issue C9, September 2007, Nicholas R. Bates

    Version of Record online : 19 SEP 2007, DOI: 10.1029/2006JC003759

  18. You have free access to this content
    Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith–Wiedemann Syndrome: Clinical Spectrum and Functional Characterization

    Human Mutation

    Volume 36, Issue 9, September 2015, Pages: 894–902, Frederic Brioude, Irène Netchine, Francoise Praz, Marilyne Le Jule, Claire Calmel, Didier Lacombe, Patrick Edery, Martin Catala, Sylvie Odent, Bertrand Isidor, Stanislas Lyonnet, Sabine Sigaudy, Bruno Leheup, Séverine Audebert-Bellanger, Lydie Burglen, Fabienne Giuliano, Jean-Luc Alessandri, Valérie Cormier-Daire, Fanny Laffargue, Sophie Blesson, Isabelle Coupier, James Lespinasse, Patricia Blanchet, Odile Boute, Clarisse Baumann, Michel Polak, Berenice Doray, Alain Verloes, Géraldine Viot, Yves Le Bouc and Sylvie Rossignol

    Version of Record online : 6 AUG 2015, DOI: 10.1002/humu.22824

  19. Clinically equivocal melanocytic skin lesions with features of regression: a dermoscopic–pathological study

    British Journal of Dermatology

    Volume 150, Issue 1, January 2004, Pages: 64–71, I. Zalaudek, G. Argenziano, G. Ferrara, H.P. Soyer, R. Corona, F. Sera, L. Cerroni, A. Carbone, A. Chiominto, L. Cicale, G. De Rosa, A. Ferrari, R. Hofmann-Wellenhof, J. Malvehy, K. Peris, M.A. Pizzichetta, S. Puig, M. Scalvenzi, S. Staibano and V. Ruocco

    Version of Record online : 26 JAN 2004, DOI: 10.1111/j.1365-2133.2004.05657.x

  20. 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

    Version of Record online : 10 MAY 2005, DOI: 10.1002/ajmg.a.30729