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There are 9482 results for: content related to: Maternal transmission of interstitial 8p23.1 deletion detected during prenatal diagnosis

  1. Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 8, August 2009, Pages: 1661–1677, Margaret J. Wat, Oleg A. Shchelochkov, Ashley M. Holder, Amy M. Breman, Aditi Dagli, Carlos Bacino, Fernando Scaglia, Roberto T. Zori, Sau Wai Cheung, Daryl A. Scott and Sung-Hae Lee Kang

    Version of Record online : 15 JUL 2009, DOI: 10.1002/ajmg.a.32896

  2. 8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients

    American Journal of Medical Genetics Part A

    Volume 161, Issue 3, March 2013, Pages: 487–500, John C.K. Barber, Jill A. Rosenfeld, Nicola Foulds, Sophie Laird, Mark S. Bateman, N. Simon Thomas, Samantha Baker, Viv K. Maloney, Arayamparambil Anilkumar, Wendy E. Smith, Valerie Banks, Sara Ellingwood, Yara Kharbutli, Lakshmi Mehta, Keith A. Eddleman, Michael Marble, Regina Zambrano, John A. Crolla and Allen N. Lamb

    Version of Record online : 23 JAN 2013, DOI: 10.1002/ajmg.a.35767

  3. 8p23.1 duplication detected by array-CGH with complete atrioventricular septal defect and unilateral hand preaxial hexadactyly

    American Journal of Medical Genetics Part A

    Volume 161, Issue 3, March 2013, Pages: 561–565, Yanliang Zhang, Ya Li, Yuming Wang, Bin Shan and Yong Duan

    Version of Record online : 12 FEB 2013, DOI: 10.1002/ajmg.a.35596

  4. Deletion of 8p23.1 with features of Cornelia de Lange syndrome and congenital diaphragmatic hernia and a review of deletions of 8p23.1 to 8pter ? A further locus for Cornelia de Lange syndrome

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 12, 15 June 2008, Pages: 1565–1570, Gareth Baynam, Jack Goldblatt and Ian Walpole

    Version of Record online : 9 MAY 2008, DOI: 10.1002/ajmg.a.32095

  5. Inside the 8p23.1 duplication syndrome; eight microduplications of likely or uncertain clinical significance

    American Journal of Medical Genetics Part A

    Volume 167, Issue 9, September 2015, Pages: 2052–2064, John C. K. Barber, Jill A. Rosenfeld, John M. Graham, Nancy Kramer, Katherine L. Lachlan, Mark S. Bateman, Morag N. Collinson, Barbro Fossøy Stadheim, Claire L. S. Turner, Jacqueline N. Gauthier, Tyler E. Reimschisel, Athar M. Qureshi, Tabib A. Dabir, Mervyn W. Humphreys, Michael Marble, Taosheng Huang, Sarah J. Beal, Joanne Massiah, Emma-Jane Taylor and Sarah L. Wynn

    Version of Record online : 11 JUN 2015, DOI: 10.1002/ajmg.a.37120

  6. Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 12, December 2012, Pages: 3148–3158, Mauro Longoni, Kasper Lage, Meaghan K. Russell, Maria Loscertales, Omar A. Abdul-Rahman, Gareth Baynam, Steven B. Bleyl, Paul D. Brady, Jeroen Breckpot, Chih P. Chen, Koenraad Devriendt, Gabriele Gillessen-Kaesbach, Arthur W. Grix, Alan F. Rope, Osamu Shimokawa, Bernarda Strauss, Dagmar Wieczorek, Elaine H. Zackai, Caroline M. Coletti, Faouzi I. Maalouf, Kristin M. Noonan, Ji H. Park, Adam A. Tracy, Charles Lee, Patricia K. Donahoe and Barbara R. Pober

    Version of Record online : 19 NOV 2012, DOI: 10.1002/ajmg.a.35665

  7. Molecular characterization of inv dup del(8p): Analysis of five cases

    American Journal of Medical Genetics Part A

    Volume 128A, Issue 2, 15 July 2004, Pages: 133–137, Osamu Shimokawa, Kenji Kurosawa, Tomoko Ida, Naoki Harada, Tatsuro Kondoh, Noriko Miyake, Kohichiro Yoshiura, Tatsuya Kishino, Tohru Ohta, Norio Niikawa and Naomichi Matsumoto

    Version of Record online : 22 APR 2004, DOI: 10.1002/ajmg.a.30063

  8. Analysis of invdupdel(8p) rearrangement: Clinical, cytogenetic and molecular characterization

    American Journal of Medical Genetics Part A

    Volume 167, Issue 5, May 2015, Pages: 1018–1025, Fe Amalia García-Santiago, Víctor Martínez-Glez, Fernando Santos, Sixto García-Miñaur, Elena Mansilla, Antonio González Meneses, Jordi Rosell, Ángeles Pérez Granero, Elena Vallespín, Luis Fernández, Blanca Sierra, María Oliver-Bonet, María Palomares, María Luisa de Torres, María Ángeles Mori, Julián Nevado, Karen E. Heath, Alicia Delicado and Pablo Lapunzina

    Version of Record online : 25 FEB 2015, DOI: 10.1002/ajmg.a.36879

  9. Allelotyping analysis at chromosome arm 8p of high-grade prostatic intraepithelial neoplasia and incidental, latent, and clinical prostate cancers

    Genes, Chromosomes and Cancer

    Volume 45, Issue 5, May 2006, Pages: 509–515, Wei Lu, Hiroyuki Takahashi, Bungo Furusato, Suguru Maekawa, Masahiro Ikegami, Akemi Sudo, Shin Egawa and Hiroshi Hano

    Version of Record online : 8 FEB 2006, DOI: 10.1002/gcc.20314

  10. Chromosome 8

    Standard Article

    eLS

    Matthew J Hilton and Dan E Wells

    Published Online : 16 JAN 2017, DOI: 10.1002/9780470015902.a0005817.pub3

  11. Linkage evidence of schizophrenia to loci near neuregulin 1 gene on chromosome 8p21 in Taiwanese families

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 134B, Issue 1, 5 April 2005, Pages: 79–83, Chih-Min Liu, Hai-Gwo Hwu, Cathy S.J. Fann, Chin-Yu Lin, Yu-Li Liu, Wen-Chen Ou-Yang and Sandy F-C Lee

    Version of Record online : 9 FEB 2005, DOI: 10.1002/ajmg.b.20161

  12. Duplication of chromosome region 8p23.1 [RIGHTWARDS ARROW] p23.3: A benign variant?

    American Journal of Medical Genetics

    Volume 91, Issue 1, 6 March 2000, Pages: 18–21, J.J.M. Engelen, U. Moog, J.L.H. Evers, H. Dassen, J.C.M. Albrechts and A.J.H. Hamers

    Version of Record online : 17 MAR 2000, DOI: 10.1002/(SICI)1096-8628(20000306)91:1<18::AID-AJMG3>3.0.CO;2-3

  13. Identification of minimal regions of deletion at 8p23.1-22 associated with metastasis of hepatocellular carcinoma

    Liver International

    Volume 27, Issue 6, August 2007, Pages: 782–790, Tomoe Lu and Hiroshi Hano

    Version of Record online : 5 JUN 2007, DOI: 10.1111/j.1478-3231.2007.01504.x

  14. Molecular cytogenetic characterization of a unique and complex de novo 8p rearrangement

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 9, 1 May 2008, Pages: 1166–1172, Susanna L. Cooke, Jill K. Northup, Neena L. Champaige, William Zinser, Paul A.W. Edwards, Lillian H. Lockhart and Gopalrao V.N. Velagaleti

    Version of Record online : 26 FEB 2008, DOI: 10.1002/ajmg.a.32248

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    High frequency of common DNA copy number abnormalities detected by bacterial artificial chromosome array comparative genomic hybridization in 24 breast cancer cell lines

    Human Cell

    Volume 22, Issue 1, February 2009, Pages: 1–10, Soichiro SAITO, Keiko MORITA and Takashi HIRANO

    Version of Record online : 12 FEB 2009, DOI: 10.1111/j.1749-0774.2008.00061.x

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    4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regions

    American Journal of Medical Genetics Part A

    Volume 170, Issue 10, October 2016, Pages: 2540–2550, Weimin Bi, Sau-Wai Cheung, Amy M. Breman and Carlos A. Bacino

    Version of Record online : 10 JUN 2016, DOI: 10.1002/ajmg.a.37796

  17. Haploinsufficiency and reduced expression of genes localized to the 8p chromosomal region in human prostate tumors

    Genes, Chromosomes and Cancer

    Volume 37, Issue 3, July 2003, Pages: 306–313, Hassan Chaib, James W. MacDonald, Robert L. Vessella, Joseph G. Washburn, Janna E. Quinn, Austin Odman, Mark A. Rubin and Jill A. Macoska

    Version of Record online : 16 APR 2003, DOI: 10.1002/gcc.10226

  18. A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 12, December 2012, Pages: 3137–3147, Cammon B. Arrington, Steven B. Bleyl, Nori Matsunami, Neil E. Bowles, Tami I. Leppert, Bradley L. Demarest, Karen Osborne, Bradley A. Yoder, Janice L. Byrne, Joshua D. Schiffman, Donald M. Null, Robert DiGeronimo, Michael Rollins, Roger Faix, Jessica Comstock, Nicola J. Camp, Mark F. Leppert, H. Joseph Yost and Luca Brunelli

    Version of Record online : 19 NOV 2012, DOI: 10.1002/ajmg.a.35664

  19. Balanced complex chromosome rearrangements: Reproductive aspects. A review

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 4, April 2012, Pages: 947–963, Kamlesh Madan

    Version of Record online : 1 MAR 2012, DOI: 10.1002/ajmg.a.35220

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    Breast cancer in young women (≤35 years): Genomic aberrations detected by comparative genomic hybridization

    International Journal of Cancer

    Volume 107, Issue 4, 20 November 2003, Pages: 583–592, Susanne Weber-Mangal, Hans-Peter Sinn, Susanne Popp, Rüdiger Klaes, Robert Emig, Martin Bentz, Ulrich Mansmann, Gunther Bastert, Claus R. Bartram and Anna Jauch

    Version of Record online : 29 AUG 2003, DOI: 10.1002/ijc.11460