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There are 28128 results for: content related to: Periventricular heterotopia with white matter abnormalities associated with 6p25 deletion

  1. Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 10, October 2012, Pages: 2430–2438, Andrée Delahaye, Suonavy Khung-Savatovsky, Azzedine Aboura, Fabien Guimiot, Séverine Drunat, Jean-Luc Alessandri, Marion Gérard, Pierre Bitoun, Julien Boumendil, Stéphanie Robin, Chan Huel, Romain Guilherme, Stéphane Serero, Pierre Gressens, Jacques Elion, Alain Verloes, Brigitte Benzacken, Anne-Lise Delezoide and Eva Pipiras

    Version of Record online : 17 AUG 2012, DOI: 10.1002/ajmg.a.35548

  2. Case of chromosome 6p25 terminal deletion associated with Axenfeld–Rieger syndrome and persistent hyperplastic primary vitreous

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 5, 1 March 2006, Pages: 503–508, Katsuhiro Suzuki, Makoto Nakamura, Emi Amano, Kumiko Mokuno, Shoichiro Shirai and Hiroko Terasaki

    Version of Record online : 6 FEB 2006, DOI: 10.1002/ajmg.a.31085

  3. The 6p subtelomere deletion syndrome

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

    Volume 145C, Issue 4, 15 November 2007, Pages: 377–382, Cheryl DeScipio

    Version of Record online : 5 OCT 2007, DOI: 10.1002/ajmg.c.30156

  4. Terminal deletion of 6p results in a recognizable phenotype

    American Journal of Medical Genetics Part A

    Volume 136A, Issue 2, 15 July 2005, Pages: 162–168, Ruth J. Lin, Athena M. Cherry, Kelly C. Chen, Michael Lyons, H. Eugene Hoyme and Louanne Hudgins

    Version of Record online : 6 JUN 2005, DOI: 10.1002/ajmg.a.30784

  5. Nine genes that may contribute to partial trisomy (6)(p22[RIGHTWARDS ARROW]pter) and unique presentation of persistent hyperplastic primary vitreous with retinal detachment

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 4, April 2012, Pages: 707–712, Pen-Hua Su, Inn-Chi Lee, Shun-Fa Yang, Yan-Yan Ng, Chan-Sheng Liu and Jia-Yuh Chen

    Version of Record online : 9 MAR 2012, DOI: 10.1002/ajmg.a.33943

  6. You have full text access to this OnlineOpen article
    Comparative methylome analysis in solid tumors reveals aberrant methylation at chromosome 6p in nasopharyngeal carcinoma

    Cancer Medicine

    Volume 4, Issue 7, July 2015, Pages: 1079–1090, Wei Dai, Arthur Kwok Leung Cheung, Josephine Mun Yee Ko, Yue Cheng, Hong Zheng, Roger Kai Cheong Ngan, Wai Tong Ng, Anne Wing Mui Lee, Chun Chung Yau, Victor Ho Fu Lee and Maria Li Lung

    Version of Record online : 29 APR 2015, DOI: 10.1002/cam4.451

  7. Axenfeld–Rieger malformation and distinctive facial features: Clues to a recognizable 6p25 microdeletion syndrome

    American Journal of Medical Genetics Part A

    Volume 132A, Issue 4, 1 February 2005, Pages: 381–385, Kenneth Maclean, James Smith, Luke St. Heaps, Nicole Chia, Rebecca Williams, Gregory B. Peters, Ella Onikul, Tim McCrossin, Ordan J. Lehmann and Lesley C. Adès

    Version of Record online : 14 JAN 2005, DOI: 10.1002/ajmg.a.30274

  8. Schizophrenia in an adult with 6p25 deletion syndrome

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 11, 1 June 2006, Pages: 1208–1213, O. Caluseriu, G. Mirza, J. Ragoussis, E.W.C. Chow, D. MacCrimmon and A.S. Bassett

    Version of Record online : 26 APR 2006, DOI: 10.1002/ajmg.a.31222

  9. Axenfeld–Rieger anomaly and Axenfeld–Rieger syndrome: Clinical, molecular-cytogenetic, and DNA array analyses of three patients with chromosomal defects at 6p25

    American Journal of Medical Genetics Part A

    Volume 155, Issue 12, December 2011, Pages: 2925–2932, Hidefumi Tonoki, Naoki Harada, Osamu Shimokawa, Ayako Yosozumi, Kadomi Monzaki, Kohei Satoh, Rika Kosaki, Atsushi Sato, Naomichi Matsumoto and Susumu Iizuka

    Version of Record online : 18 OCT 2011, DOI: 10.1002/ajmg.a.33858

  10. Subtelomeric deletions of chromosome 6p: Molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher–Schinzel (3C) syndrome

    American Journal of Medical Genetics Part A

    Volume 134A, Issue 1, 1 April 2005, Pages: 3–11, Cheryl DeScipio, Lori Schneider, Terri L. Young, Nora Wasserman, Dinah Yaeger, Fengmin Lu, Patricia G. Wheeler, Marc S. Williams, Lynn Bason, Lori Jukofsky, Ammini Menon, Ryan Geschwindt, Albert E. Chudley, Jorge Saraiva, Albert A. G. L. Schinzel, Agnes Guichet, William E. Dobyns, Annick Toutain, Nancy B. Spinner and Ian D. Krantz

    Version of Record online : 9 FEB 2005, DOI: 10.1002/ajmg.a.30573

  11. Epiphyseal dysplasia and other skeletal anomalies in a patient with the 6p25 microdeletion syndrome

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 18, 15 September 2006, Pages: 1955–1959, Peter Kannu, Paul Oei, Howard R. Slater, Ouda Khammy and Salim Aftimos

    Version of Record online : 11 AUG 2006, DOI: 10.1002/ajmg.a.31411

  12. Renal complications in 6p duplication syndrome: Microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS)

    American Journal of Medical Genetics Part A

    Volume 167, Issue 3, March 2015, Pages: 592–601, Megumi Yoshimura-Furuhata, Akira Nishimura-Tadaki, Yoshiro Amano, Takashi Ehara, Yuko Hamasaki, Masaki Muramatsu, Seiichiro Shishido, Atsushi Aikawa, Riku Hamada, Kenji Ishikura, Hiroshi Hataya, Yoshihiko Hidaka, Shunsuke Noda, Kenichi Koike, Keiko Wakui, Yoshimitsu Fukushima, Naomichi Matsumoto, Midori Awazu, Noriko Miyake and Tomoki Kosho

    Version of Record online : 18 FEB 2015, DOI: 10.1002/ajmg.a.36942

  13. A review of association and linkage studies for genetical analyses of learning disorders

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 7, 5 October 2007, Pages: 923–943, Emrah Caylak

    Version of Record online : 17 MAY 2007, DOI: 10.1002/ajmg.b.30537

  14. A family with a complex clinical presentation characterized by arrhythmogenic right ventricular dysplasia/cardiomyopathy and features of branchio-oculo-facial syndrome

    American Journal of Medical Genetics Part A

    Volume 161, Issue 2, February 2013, Pages: 371–376, Brittney Murray, Rohan Wagle, Nuria Amat-Alarcon, Alisha Wilkens, Paul Stephens, Elaine H. Zackai, Elizabeth Goldmuntz, Hugh Calkins, Matthew A. Deardorff and Daniel P. Judge

    Version of Record online : 10 JAN 2013, DOI: 10.1002/ajmg.a.35733

  15. Array-CGH and clinical characterization in a patient with subtelomeric 6p deletion without ocular dysgenesis

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 1, January 2012, Pages: 150–154, Maria Piccione, R. Antona, E. Salzano, S. Cavani, M. Malacarne, R. Morreale Bubella, M. Pierluigi, C.D. Viaggi and Giovanni Corsello

    Version of Record online : 21 NOV 2011, DOI: 10.1002/ajmg.a.34308

  16. You have free access to this content
    Clustering by neurocognition for fine mapping of the schizophrenia susceptibility loci on chromosome 6p

    Genes, Brain and Behavior

    Volume 8, Issue 8, November 2009, Pages: 785–794, S.-H. Lin, C. -M. Liu, Y. -L. Liu, C. Shen-Jang Fann, P. -C. Hsiao, J. -Y. Wu, S. -I. Hung, C. -H. Chen, H. -M. Wu, Y. -S. Jou, S. K. Liu, T. J. Hwang, M. H. Hsieh, C. -C. Chang, W. -C. Yang, J. -J. Lin, F. H. -C. Chou, S. V. Faraone, M. T. Tsuang, H. -G. Hwu and W. J. Chen

    Version of Record online : 21 JUL 2009, DOI: 10.1111/j.1601-183X.2009.00523.x

  17. Primary cutaneous anaplastic large cell lymphomas with 6p25.3 rearrangement exhibit particular histological features

    Histopathology

    Volume 66, Issue 6, May 2015, Pages: 846–855, Arantza Onaindia, Santiago Montes-Moreno, Socorro M Rodríguez-Pinilla, Ana Batlle, Sonia González de Villambrosía, Antonio M Rodríguez, Víctor Alegre, Glenda M Bermúdez, Carmen González-Vela and Miguel A Piris

    Version of Record online : 4 FEB 2015, DOI: 10.1111/his.12529

  18. Mild developmental delay in terminal chromosome 6p deletion

    American Journal of Medical Genetics Part A

    Volume 129A, Issue 2, 30 August 2004, Pages: 201–205, Kelly M. Chen, Athena M. Cherry, Jin S. Hahn and Gregory M. Enns

    Version of Record online : 8 JUL 2004, DOI: 10.1002/ajmg.a.30127

  19. You have free access to this content
    The Human Obesity Gene Map: The 2005 Update

    Obesity

    Volume 14, Issue 4, April 2006, Pages: 529–644, Tuomo Rankinen, Aamir Zuberi, Yvon C. Chagnon, S. John Weisnagel, George Argyropoulos, Brandon Walts, Louis Pérusse and Claude Bouchard

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2006.71

  20. FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6

    American Journal of Medical Genetics Part A

    Volume 124A, Issue 3, 30 January 2004, Pages: 280–287, Hui Z. Zhang, Peining Li, Dongmei Wang, Shannon Huff, Manjunath Nimmakayalu, Mazin Qumsiyeh and Barbara R. Pober

    Version of Record online : 31 JUL 2003, DOI: 10.1002/ajmg.a.20413