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There are 28577 results for: content related to: Duplication of 18q21.32–q22.3 identified in a stillborn and two relatives with minimal dysmorphic features

  1. Genotype–phenotype mapping of chromosome 18q deletions by high-resolution array CGH: An update of the phenotypic map

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 16, 15 August 2007, Pages: 1858–1867, Ilse Feenstra, Lisenka E.L.M. Vissers, Mirjam Orsel, Ad Geurts van Kessel, Han G. Brunner, Joris A. Veltman and Conny M.A. van Ravenswaaij-Arts

    Version of Record online : 13 JUL 2007, DOI: 10.1002/ajmg.a.31850

  2. Duplication 18q21.31-q22.2

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 4, 15 February 2007, Pages: 343–348, Caterina Ceccarini, Lorenzo Sinibaldi, Laura Bernardini, Roberto De Simone, Rita Mingarelli, Antonio Novelli and Bruno Dallapiccola

    Version of Record online : 26 JAN 2007, DOI: 10.1002/ajmg.a.31588

  3. Involvement of mutations in the DPC4 promoter in endometrial carcinoma development

    Molecular Carcinogenesis

    Volume 25, Issue 1, May 1999, Pages: 64–72, Yong Zhou, Hidenori Kato, Dan Shan, Rieko Minami, Sohei Kitazawa, Takao Matsuda, Takahiro Arima, J. Carl Barrett and Norio Wake

    Version of Record online : 12 MAY 1999, DOI: 10.1002/(SICI)1098-2744(199905)25:1<64::AID-MC8>3.0.CO;2-Z

  4. Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18

    American Journal of Medical Genetics

    Volume 101, Issue 3, 1 July 2001, Pages: 226–239, Paweł Stankiewicz, Izabela Brozek, Zofia Hélias-Rodzewicz, Jolanta Wierzba, Jacek Pilch, Ewa Bocian, Anna Balcerska, Agnieszka Woźniak, Iwona Kardaś, Jutta Wirth, Tadeusz Mazurczak and Janusz Limon

    Version of Record online : 11 JUN 2001, DOI: 10.1002/1096-8628(20010701)101:3<226::AID-AJMG1349>3.0.CO;2-#

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    Frequent Allelic Imbalance on Chromosome 18q21 in Early Superficial Colorectal Cancers

    Japanese Journal of Cancer Research

    Volume 90, Issue 12, December 1999, Pages: 1329–1337, Yoshimitsu Akiyama, Takehiro Arai, Hiromi Nagasaki, Osmar Kenji Yagi, Atsuko Nakahata, Tomoko Nakajima, Yasuo Ohkura, Takehisa Iwai, Kiyoshi Saitoh and Yasuhito Yuasa

    Version of Record online : 23 AUG 2005, DOI: 10.1111/j.1349-7006.1999.tb00716.x

  6. Deletion of chromosome region 18q21.1 [RIGHTWARDS ARROW] 18q21.3 in a patient without clinical features of the 18q- phenotype

    American Journal of Medical Genetics Part A

    Volume 119A, Issue 3, 15 June 2003, Pages: 356–359, J.J.M. Engelen, U. Moog, J. Weber, A.A.M. Haagen, C.M.J. van Uum and A.J.H. Hamers

    Version of Record online : 15 JAN 2003, DOI: 10.1002/ajmg.a.10266

  7. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: Data from United States and Canadian laboratories

    American Journal of Medical Genetics

    Volume 33, Issue 1, May 1989, Pages: 14–53, Dr. Art Daniel, Ernest B. Hook and Gary Wulf

    Version of Record online : 5 JUN 2005, DOI: 10.1002/ajmg.1320330105

  8. You have free access to this content
    Delineation of the breakpoint at 18q21.1 in a cell line (KARPAS1106) derived from mediastinal B-cell lymphoma by fluorescencein situ hybridization with multiple YAC clones

    International Journal of Cancer

    Volume 78, Issue 1, 25 September 1998, Pages: 100–105, Akiko Tamura, Tomoaki Akagi, Naozo Nakazawa, Kei Kashima, Shigeo Nakamura, Abraham Karpas, Gary A. Silverman, Yasuo Morishima, Masafumi Taniwaki and Masao Seto

    Version of Record online : 6 JAN 1999, DOI: 10.1002/(SICI)1097-0215(19980925)78:1<100::AID-IJC16>3.0.CO;2-F

  9. Molecular characterization of a patient with central nervous system dysmyelination and cryptic unbalanced translocation between chromosomes 4q and 18q

    American Journal of Medical Genetics Part A

    Volume 120A, Issue 1, 1 July 2003, Pages: 127–135, Shelly R. Gunn, Mansoor Mohammed, Xavier T. Reveles, David H. Viskochil, Janice C. Palumbos, Teresa L. Johnson-Pais, Daniel E. Hale, Jack L. Lancaster, L. Jean Hardies, Odile Boespflug-Tanguy, Jannine D. Cody and Robin J. Leach

    Version of Record online : 25 FEB 2003, DOI: 10.1002/ajmg.a.20026

  10. Beckwith–Wiedemann-like macroglossia and 18q23 haploinsufficiency

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 23, 1 December 2007, Pages: 2796–2803, Frédéric Lirussi, Laurence Jonard, Véronique Gaston, Damien Sanlaville, R. Frank Kooy, Birgitta Winnepenninckx, Eamonn R. Maher, David R. FitzPatrick, Christine Gicquel, Marie-France Portnoï, Rémy Couderc, Marie-Paule Vazquez and Michel Bahuau

    Version of Record online : 9 NOV 2007, DOI: 10.1002/ajmg.a.31768

  11. Array-based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 11, 1 June 2006, Pages: 1156–1163, P.A. Lennon, M.L. Cooper, M.A. Curtis, C. Lim, Z. Ou, A. Patel, S.W. Cheung and C.A. Bacino

    Version of Record online : 10 MAY 2006, DOI: 10.1002/ajmg.a.31243

  12. Mosaic 18q21.2 deletions including the TCF4 gene: A clinical report

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 12, December 2012, Pages: 3174–3181, Massimiliano Rossi, Audrey Labalme, Marie-Pierre Cordier, Marianne Till, Gaëlle Blanchard, Remi Dubois, Laurent Guibaud, Sophie Heissat, Etienne Javouhey, Alain Lachaux, Pierre-Yves Mure, Dorothée Ville, Patrick Edery and Damien Sanlaville

    Version of Record online : 19 NOV 2012, DOI: 10.1002/ajmg.a.35588

  13. 18q21 rearrangement in diffuse large cell lymphoma: incidence and clinical significance

    British Journal of Haematology

    Volume 72, Issue 2, June 1989, Pages: 178–183, Kenneth Offit, Prasad R. K. Koduru, Rachel Hollis, Daniel Filippa, Suresh C. Jhanwar, Bayard C. Clarkson and R. S. K. Chaganti

    Version of Record online : 12 MAR 2008, DOI: 10.1111/j.1365-2141.1989.tb07680.x

  14. First non-mosaic case of isopseudodicentric chromosome 18 (psu idic(18)(pter [RIGHTWARDS ARROW] q22.1::q22.1 [RIGHTWARDS ARROW] pter) Is associated with multiple congenital anomalies reminiscent of trisomy 18 and 18q− syndrome

    American Journal of Medical Genetics Part A

    Volume 127A, Issue 1, 15 May 2004, Pages: 58–64, M. Meins, D. Böhm, A. Großmann, E. Herting, B. Fleckenstein, C. Fauth, M.R. Speicher, R. Schindler, B. Zoll, I. Bartels and Peter Burfeind

    Version of Record online : 26 NOV 2003, DOI: 10.1002/ajmg.a.20644

  15. Chromosome 18q paracentric inversion in a family with mental retardation and hearing loss

    American Journal of Medical Genetics

    Volume 76, Issue 5, 13 April 1998, Pages: 372–378, Kim M. Keppler-Noreuil, Andrew J. Carroll, Sara C. Finley, Maria Descartes, Jannine D. Cody, Barbara R. DuPont, Charles T. Gay and Robin J. Leach

    Version of Record online : 6 JAN 1999, DOI: 10.1002/(SICI)1096-8628(19980413)76:5<372::AID-AJMG2>3.0.CO;2-P

  16. Loss of heterozygosity at 18q21 region in gastric cancer involves a number of cancer-related genes and correlates with stage and histology, but lacks independent prognostic value

    The Journal of Pathology

    Volume 197, Issue 1, May 2002, Pages: 44–50, M. E. Candusso, O. Luinetti, L. Villani, P. Alberizzi, C. Klersy, R. Fiocca, G. N. Ranzani and E. Solcia

    Version of Record online : 19 MAR 2002, DOI: 10.1002/path.1105

  17. Prospective risk in reciprocal translocation heterozygotes at amniocentesis as determined by potential chromosome imbalance sizes. Data of the european collaborative prenatal diagnosis centres

    Prenatal Diagnosis

    Volume 6, Issue 5, September/October 1986, Pages: 315–350, Dr. A. Daniel, A. Boué and P. Gallano

    Version of Record online : 21 NOV 2005, DOI: 10.1002/pd.1970060502

  18. Familial 4.8 MB deletion on 18q23 associated with growth hormone insufficiency and phenotypic variability

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 3, March 2012, Pages: 611–616, Ester Margarit, Carme Morales, Laia Rodríguez-Revenga, Raquel Monné, Cèlia Badenas, Anna Soler, Núria Clusellas, Irene Mademont and Aurora Sánchez

    Version of Record online : 2 FEB 2012, DOI: 10.1002/ajmg.a.34221

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    Identification of a characteristic copy number alteration profile by high-resolution single nucleotide polymorphism arrays associated with metastatic sporadic colorectal cancer

    Cancer

    Volume 120, Issue 13, 1 July 2014, Pages: 1948–1959, María González-González, Celia Fontanillo, María M. Abad, María L. Gutiérrez, Ines Mota, Oscar Bengoechea, Ángel Santos-Briz, Oscar Blanco, Emilio Fonseca, Juana Ciudad, Manuel Fuentes, Javier De Las Rivas, José A. Alcazar, Jacinto García, Luís Muñoz-Bellvis, Alberto Orfao and José M. Sayagués

    Version of Record online : 25 MAR 2014, DOI: 10.1002/cncr.28681

  20. 18q deletions: Clinical, molecular, and brain MRI findings of 14 individuals

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 4, 15 February 2006, Pages: 331–339, Tarja Linnankivi, Pentti Tienari, Mirja Somer, Marketta Kähkönen, Tuula Lönnqvist, Leena Valanne and Helena Pihko

    Version of Record online : 17 JAN 2006, DOI: 10.1002/ajmg.a.31072