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There are 7441 results for: content related to: Interstitial deletion of the short arm of chromosome 10 del(10)(p11.2p12.32) in a patient with congenital heart disease, minor dysmorphism, and mental retardation

  1. Clinical description of a patient carrying the smallest reported deletion involving 10p14 region

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 4, April 2012, Pages: 832–835, Daniela Melis, Rita Genesio, Pasquale Boemio, Ennio Del Giudice, Gerarda Cappuccio, Angela Mormile, Valentina Ronga, Anna Conti, Floriana Imperati, Lucio Nitsch and Generoso Andria

    Version of Record online : 9 MAR 2012, DOI: 10.1002/ajmg.a.34133

  2. Molecular and clinical characterization of patients with overlapping 10p deletions

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 5, May 2010, Pages: 1233–1243, Anna Lindstrand, Helena Malmgren, Annapia Verri, Elisa Benetti, Maud Eriksson, Ann Nordgren, Britt-Marie Anderlid, Irina Golovleva, Jacqueline Schoumans and Elisabeth Blennow

    Version of Record online : 13 APR 2010, DOI: 10.1002/ajmg.a.33366

  3. Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome

    Clinical Genetics

    Volume 66, Issue 2, August 2004, Pages: 128–136, SA Yatsenko, AN Yatsenko, K Szigeti, WJ Craigen, P Stankiewicz, SW Cheung and JR Lupski

    Version of Record online : 25 JUN 2004, DOI: 10.1111/j.1399-0004.2004.00290.x

  4. Interstitial 10p11.23–p12.1 microdeletions associated with developmental delay, craniofacial abnormalities, and cryptorchidism

    American Journal of Medical Genetics Part A

    Volume 164, Issue 10, October 2014, Pages: 2623–2626, Henry J. Mroczkowski, Georgianne Arnold, Francis X. Schneck, Aleksandar Rajkovic and Svetlana A. Yatsenko

    Version of Record online : 29 JUL 2014, DOI: 10.1002/ajmg.a.36627

  5. You have full text access to this OnlineOpen article
    Clinical description of a neonate carrying the largest reported deletion involving the 10p15.3p13 region

    Clinical Case Reports

    Volume 5, Issue 8, August 2017, Pages: 1369–1375, Saet Byeol Kim, Young-Eun Kim, Ji Mi Jung, Hye Young Jin, Yun-Jung Lim and Mi Lim Chung

    Version of Record online : 11 JUL 2017, DOI: 10.1002/ccr3.1070

  6. Pseudoarthrosis of the clavicle and copper beaten skull associated with chromosome 10p11.21p12.1 microdeletion

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 2, 15 January 2008, Pages: 233–237, Raveen Shahdadpuri, Bert de Vries, Rolph Pfundt, Nicole de Leeuw and William Reardon

    Version of Record online : 13 DEC 2007, DOI: 10.1002/ajmg.a.32088

  7. Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 9, September 2010, Pages: 2327–2334, Ni-Chung Lee, Ming Chen, Gwo-Chin Ma, Dong-Jay Lee, Tzu-Jou Wang, Yu-Yuan Ke, Yin-Hsiu Chien and Wuh-Liang Hwu

    Version of Record online : 3 AUG 2010, DOI: 10.1002/ajmg.a.33581

  8. Hypervalent Compounds of Organic Germanium, Tin and Lead Derivatives

    The Chemistry of Organic Germanium, Tin and Lead Compounds, Volume 2

    Yuri I. Baukov, Stanislav N. Tandura, Pages: 963–1239, 2003

    Published Online : 5 FEB 2003, DOI: 10.1002/0470857188.ch16

  9. Discrete–continuous analysis of optimal equipment replacement

    International Transactions in Operational Research

    Volume 17, Issue 5, September 2010, Pages: 577–593, Yuri Yatsenko and Natali Hritonenko

    Version of Record online : 11 FEB 2010, DOI: 10.1111/j.1475-3995.2009.00747.x

  10. 10q26.1 Microdeletion: Redefining the critical regions for microcephaly and genital anomalies

    American Journal of Medical Genetics Part A

    Volume 167, Issue 11, November 2015, Pages: 2707–2713, Nancy Choucair, Joelle Abou Ghoch, Ali Fawaz, André Mégarbané and Eliane Chouery

    Version of Record online : 26 JUN 2015, DOI: 10.1002/ajmg.a.37211

  11. Co-occurrence of 22q11 deletion syndrome and hdr syndrome

    American Journal of Medical Genetics Part A

    Volume 161, Issue 10, October 2013, Pages: 2576–2581, Ryoko Fukai, Nobuhiko Ochi, Akira Murakami, Mitsuko Nakashima, Yoshinori Tsurusaki, Hirotomo Saitsu, Naomichi Matsumoto and Noriko Miyake

    Version of Record online : 5 AUG 2013, DOI: 10.1002/ajmg.a.36083

  12. Chromosome 10

    Standard Article


    Theologia Sarafidou and Nicholas Moschonas

    Published Online : 6 MAR 2017, DOI: 10.1002/9780470015902.a0005819.pub3

  13. You have free access to this content
    High resolution SNP array genomic profiling of peripheral T cell lymphomas, not otherwise specified, identifies a subgroup with chromosomal aberrations affecting the REL locus

    British Journal of Haematology

    Volume 148, Issue 3, February 2010, Pages: 402–412, Sylvia Hartmann, Stefan Gesk, René Scholtysik, Markus Kreuz, Stefanie Bug, Inga Vater, Claudia Döring, Sergio Cogliatti, Marie Parrens, Jean-Philippe Merlio, Anna Kwiecinska, Anna Porwit, Pier Paolo Piccaluga, Stefano Pileri, Gerald Hoefler, Ralf Küppers, Reiner Siebert and Martin-Leo Hansmann

    Version of Record online : 22 OCT 2009, DOI: 10.1111/j.1365-2141.2009.07956.x

  14. Interstitial 10p deletion derived from a maternal ins(16;10)(q22;p13p15.2): Report of the first familial case of 10p monosomy affecting to two familial members of different generations

    American Journal of Medical Genetics Part A

    Volume 170, Issue 5, May 2016, Pages: 1268–1273, Raquel M. Fernández, Javier Sánchez, Lutgardo García-Díaz, Yolanda Peláez-Nora, Antonio González-Meneses, Guillermo Antiñolo and Salud Borrego

    Version of Record online : 14 JAN 2016, DOI: 10.1002/ajmg.a.37559

  15. NMR Study of Intrinsic Defects in Congruent Lithium Niobate

    Crystal Research and Technology

    Volume 34, Issue 5-6, June 1999, Pages: 709–713, A. Yatsenko, H. Maksimova and N. Sergeev

    Version of Record online : 7 JUN 1999, DOI: 10.1002/(SICI)1521-4079(199906)34:5/6<709::AID-CRAT709>3.0.CO;2-X

  16. Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feet

    American Journal of Medical Genetics Part A

    Volume 173, Issue 6, June 2017, Pages: 1611–1619, Melanie Lacaria, Myriam Srour, Jacques L. Michaud, Asif Doja, Elka Miller, Jeremy Schwartzentruber, Claire Goldsmith, Jacek Majewski, FORGE Canada Consortium and Kym M. Boycott

    Version of Record online : 21 APR 2017, DOI: 10.1002/ajmg.a.38231

  17. Subtelomeric deletion of chromosome 10p15.3: Clinical findings and molecular cytogenetic characterization

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 9, September 2012, Pages: 2152–2161, Cheryl DeScipio, Laura Conlin, Jill Rosenfeld, James Tepperberg, Romela Pasion, Ankita Patel, Marie T. McDonald, Swaroop Aradhya, Darlene Ho, Jennifer Goldstein, Marianne McGuire, Surabhi Mulchandani, Livija Medne, Rosemarie Rupps, Alvaro H. Serrano, Erik C. Thorland, Anne C.-H. Tsai, Yvonne Hilhorst-Hofstee, Claudia A.L. Ruivenkamp, Hilde Van Esch, Marie-Claude Addor, Danielle Martinet, Thornton B.A. Mason, Dinah Clark, Nancy B. Spinner and Ian D. Krantz

    Version of Record online : 27 JUL 2012, DOI: 10.1002/ajmg.a.35574

  18. Hypervalent Compounds of Organic Germanium, Tin and Lead Derivatives

    Standard Article

    Patai's Chemistry of Functional Groups

    Yuri I. Baukov and Stanislav N. Tandura

    Published Online : 15 DEC 2009, DOI: 10.1002/9780470682531.pat0268

  19. A de novo 10p11.23-p12.1 deletion recapitulates the phenotype observed in WAC mutations and strengthens the role of WAC in intellectual disability and behavior disorders

    American Journal of Medical Genetics Part A

    Volume 170, Issue 7, July 2016, Pages: 1912–1917, Fatma Abdelhedi, Laila El Khattabi, Nouha Essid, Geraldine Viot, Dominique Letessier, Aziza Lebbar and Jean-Michel Dupont

    Version of Record online : 27 APR 2016, DOI: 10.1002/ajmg.a.37686

  20. A novel contiguous gene deletion of AVPR2 and ARHGAP4 genes in male dizygotic twins with nephrogenic diabetes insipidus and intellectual disability

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 10, October 2012, Pages: 2511–2518, Lingli Huang, Gemma Poke, Jozef Gecz and Kate Gibson

    Version of Record online : 10 SEP 2012, DOI: 10.1002/ajmg.a.35591