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There are 133233 results for: content related to: Transmitted deletions of medial 5p and learning difficulties; Does the cadherin cluster only become penetrant when flanking genes are deleted?

  1. Characterization of a de novo complex chromosomal rearrangement in a patient with cri-du-chat and trisomy 5p syndromes

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 11, November 2009, Pages: 2513–2521, Ascensión Vera-Carbonell, Juan Antonio Bafalliu, Encarna Guillén-Navarro, Ariadna Escalona, María J. Ballesta-Martínez, Carme Fuster, Asunción Fernández and Isabel López-Expósito

    Version of Record online : 19 OCT 2009, DOI: 10.1002/ajmg.a.33055

  2. Implications of prenatal diagnosis of the fetus with both interstitial deletion and a small marker ring originating from chromosome 5

    American Journal of Medical Genetics Part A

    Volume 155, Issue 1, January 2011, Pages: 192–196, Hiroyasu Ohashi, Kaoru Suzumori, Yasushi Chisaka, Shinichi Sonta, Tomoko Kobayashi, Yoko Aoki, Yoichi Matsubara, Michiko Sone and Lisa G. Shaffer

    Version of Record online : 28 DEC 2010, DOI: 10.1002/ajmg.a.33764

  3. 5p deletions: Current knowledge and future directions

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

    Volume 169, Issue 3, September 2015, Pages: 224–238, Joanne M. Nguyen, Krista J. Qualmann, Rebecca Okashah, AmySue Reilly, Mikhail F. Alexeyev and Dennis J. Campbell

    Version of Record online : 3 AUG 2015, DOI: 10.1002/ajmg.c.31444

  4. Gain and overexpression of the oncostatin M receptor occur frequently in cervical squamous cell carcinoma and are associated with adverse clinical outcome

    The Journal of Pathology

    Volume 212, Issue 3, July 2007, Pages: 325–334, G Ng, D Winder, B Muralidhar, E Gooding, I Roberts, M Pett, G Mukherjee, J Huang and N Coleman

    Version of Record online : 22 MAY 2007, DOI: 10.1002/path.2184

  5. Supernumerary marker chromosomes 5: Confirmation of a critical region and resultant phenotype

    American Journal of Medical Genetics

    Volume 111, Issue 1, 22 July 2002, Pages: 19–26, Loredana D'Amato Sizonenko, Daniel Ng, Paul Oei and Ingrid Winship

    Version of Record online : 21 JUN 2002, DOI: 10.1002/ajmg.10459

  6. Multigenerational autosomal dominant inheritance of 5p chromosomal deletions

    American Journal of Medical Genetics Part A

    Volume 170, Issue 3, March 2016, Pages: 583–593, Bin Zhang, Marcia Willing, Dorothy K. Grange, Marwan Shinawi, Linda Manwaring, Marisa Vineyard, Shashikant Kulkarni and Catherine E. Cottrell

    Version of Record online : 24 NOV 2015, DOI: 10.1002/ajmg.a.37445

  7. Amplification of 3q26 and 5p15 regions in cervical intraepithelial neoplasia

    Acta Obstetricia et Gynecologica Scandinavica

    Volume 93, Issue 10, October 2014, Pages: 997–1002, Erik Kudela, Anna Farkasova, Jozef Visnovsky, Tomas Balharek, Petra Sumichrastova, Jana Sivakova, Lukas Plank and Jan Danko

    Version of Record online : 17 SEP 2014, DOI: 10.1111/aogs.12485

  8. You have free access to this content
    Loss of heterozygosity analysis on chromosome 5p defines 5p13-12 as the critical region involved in tumor progression of bladder carcinomas

    International Journal of Cancer

    Volume 89, Issue 2, 20 March 2000, Pages: 194–197, Malte Böhm, Rainer Kleine-Besten and Ilse Wieland

    Version of Record online : 6 APR 2000, DOI: 10.1002/(SICI)1097-0215(20000320)89:2<194::AID-IJC15>3.0.CO;2-S

  9. A new genomic mechanism leading to cri-du-chat syndrome

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 24, 15 December 2006, Pages: 2714–2720, Sarah T. South, Jeffrey J. Swensen, Teresa Maxwell, Alan Rope, Arthur R. Brothman and Zhong Chen

    Version of Record online : 13 NOV 2006, DOI: 10.1002/ajmg.a.31496

  10. Inverted duplication with terminal deletion of 5p and no cat-like cry

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 9, 1 May 2008, Pages: 1173–1179, Jia-Chi Wang, Bradley P. Coe, Brenda Lomax, Patrick M. MacLeod, Malcolm I. Parslow, Jacqueline E. Schein, Wan L. Lam and Patrice Eydoux

    Version of Record online : 11 FEB 2008, DOI: 10.1002/ajmg.a.32246

  11. Unusual isochromosome 5p marker chromosome

    American Journal of Medical Genetics Part A

    Volume 167, Issue 2, February 2015, Pages: 455–459, Fanny Roulet-Coudrier, Amine Rouibi, Clotilde Thuillier, Sylvie Bourthoumieu, Aziza Lebbar, Jean-Michel Dupont and Catherine Yardin

    Version of Record online : 25 NOV 2014, DOI: 10.1002/ajmg.a.36843

  12. You have free access to this content
    Stratification of pedigrees multiplex for systemic lupus erythematosus and for self-reported rheumatoid arthritis detects a systemic lupus erythematosus susceptibility gene (SLER1) at 5p15.3

    Arthritis & Rheumatism

    Volume 46, Issue 11, November 2002, Pages: 2937–2945, Bahram Namjou, Swapan K. Nath, Jeff Kilpatrick, Jennifer A. Kelly, Jeff Reid, Judith A. James and John B. Harley

    Version of Record online : 8 NOV 2002, DOI: 10.1002/art.10588

  13. Electroclinical and cytogenetic features of epilepsy in cri-du-chat syndrome

    Epileptic Disorders

    Volume 17, Issue 4, December 2015, Pages: 485–490, Yukako Nakagami, Kiyohito Terada, Hitoshi Ikeda, Toshio Hiyoshi and Yushi Inoue

    Version of Record online : 25 JAN 2016, DOI: 10.1684/epd.2015.0780

  14. CHANGE AND THE ETERNAL PART OF THE MIND IN SPINOZA

    Pacific Philosophical Quarterly

    Volume 91, Issue 3, September 2010, Pages: 369–384, MICHAEL LEBUFFE

    Version of Record online : 1 SEP 2010, DOI: 10.1111/j.1468-0114.2010.01372.x

  15. FISH analysis of terminal deletions in patients diagnosed with cri-du-chat syndrome

    Clinical Genetics

    Volume 56, Issue 4, October 1999, Pages: 282–288, R Catrinel Marinescu, Elizabeth I Johnson, Deborah Grady, Xiao-Ning Chen and Joan Overhauser

    Version of Record online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.1999.560405.x

  16. Trisomy of the short arm of chromosome 5 due to a de novo inversion and duplication (5)(p15.3 p13.3)

    American Journal of Medical Genetics Part A

    Volume 136A, Issue 4, 1 August 2005, Pages: 381–385, M. Cervera, S. Sánchez, B. Molina, M.A. Alcántara, V. Del Castillo, A. Carnevale and A. González-del Angel

    Version of Record online : 6 JUL 2005, DOI: 10.1002/ajmg.a.30791

  17. Replication of results of genome-wide association studies on lung cancer susceptibility loci in a Korean population

    Respirology

    Volume 17, Issue 4, May 2012, Pages: 699–706, EUN YOUNG BAE, SHIN YUP LEE, BONG KYOON KANG, EUN JIN LEE, YI YOUNG CHOI, HYO-GYOUNG KANG, JIN EUN CHOI, HYO-SUNG JEON, WON KEE LEE, SHIN KAM, KYUNG MIN SHIN, GUANG JIN, SEUNG SOO YOO, JAEHEE LEE, SEUNG ICK CHA, CHANG HO KIM, TAE HOON JUNG and JAE YONG PARK

    Version of Record online : 19 APR 2012, DOI: 10.1111/j.1440-1843.2012.02165.x

  18. Identification of a dup(5)(p15.3) by multicolor banding

    Clinical Genetics

    Volume 61, Issue 4, April 2002, Pages: 277–282, D Riordan, A Vust, DE Wickstrom, J Brown, AE Chudley, D Tomkins, I Chudoba and AJ Dawson

    Version of Record online : 27 MAY 2002, DOI: 10.1034/j.1399-0004.2002.610406.x

  19. Rapid array-based genomic characterization of a subtle structural abnormality: A patient with psychosis and der(18)t(5;18)(p14.1;p11.23)

    American Journal of Medical Genetics Part A

    Volume 134A, Issue 3, 30 April 2005, Pages: 282–289, Carolyn M. Drazinic, Adife G. Ercan-Sencicek, Laura M. Gault, Fuki M. Hisama, Mazin B. Qumsiyeh, Norma J. Nowak, Joseph F. Cubells and Matthew W. State

    Version of Record online : 7 MAR 2005, DOI: 10.1002/ajmg.a.30616

  20. Cytogenetic and molecular characterization of a three-generation family with chromosome 5p terminal deletion

    Clinical Genetics

    Volume 73, Issue 6, June 2008, Pages: 585–590, J-S Fang, K-F Lee, C-T Huang, C-L Syu, K-J Yang, L-H Wang, D-L Liao and C-H Chen

    Version of Record online : 9 APR 2008, DOI: 10.1111/j.1399-0004.2008.00995.x