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There are 28962 results for: content related to: Significant linkage to chromosome 22q for exploratory eye movement dysfunction in schizophrenia

  1. Affected sibling pair linkage analysis of qualitative and quantitative traits for schizophrenia on chromosome 22 in a Chinese population

    American Journal of Medical Genetics

    Volume 105, Issue 4, 8 May 2001, Pages: 321–327, Guiqing Cai, Tao Li, Hong Deng, Jinghua Zhao, Xun Hu, Robin M. Murray, Xiehe Liu, Pak C. Sham and David A. Collier

    Article first published online : 30 APR 2001, DOI: 10.1002/ajmg.1346

  2. Search for common haplotypes on chromosome 22q in patients with schizophrenia or bipolar disorder from the Faroe Islands

    American Journal of Medical Genetics

    Volume 114, Issue 2, 8 March 2002, Pages: 245–252, T.H. Jorgensen, A.D. Børglum, O. Mors, A.G. Wang, M. Pinaud, T.J. Flint, H.A. Dahl, M. Vang, T.A. Kruse and H. Ewald

    Article first published online : 9 JAN 2002, DOI: 10.1002/ajmg.10191

  3. Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method

    Pediatrics International

    Volume 44, Issue 3, June 2002, Pages: 264–268, Yi-Ru Shi, Kai-Sheng Hsieh, Jer-Yuarn Wu, Cheng-Chun Lee, Chang-Hai Tsai and Fuu-Jen Tsai

    Article first published online : 6 JUN 2002, DOI: 10.1046/j.1442-200X.2002.01553.x

  4. You have free access to this content
    Impairment of exploratory eye movement in schizophrenia patients and their siblings

    Psychiatry and Clinical Neurosciences

    Volume 62, Issue 5, October 2008, Pages: 487–493, Sakae Takahashi, Eiichi Tanabe, Kazuo Yara, Masato Matsuura, Eisuke Matsushima and Takuya Kojima

    Article first published online : 29 SEP 2008, DOI: 10.1111/j.1440-1819.2008.01840.x

  5. Localization of a putative low-penetrance ependymoma susceptibility locus to 22q11 using a chromosome 22 tiling-path genomic microarray

    Genes, Chromosomes and Cancer

    Volume 43, Issue 4, August 2005, Pages: 329–338, Anneke C. J. Ammerlaan, Cecilia de Bustos, Abdelhay Ararou, Patrick G. Buckley, Kiran K. Mantripragada, Marco J. Verstegen, Theo J. M. Hulsebos and Jan P. Dumanski

    Article first published online : 3 MAY 2005, DOI: 10.1002/gcc.20207

  6. DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion

    American Journal of Medical Genetics Part A

    Volume 117A, Issue 1, 15 February 2003, Pages: 1–5, Oliver Bartsch, Michaela Nemecková, Eduard Kocárek, Annett Wagner, Alena Puchmajerová, Maja Poppe, Katrin Ounap and Petr Goetz

    Article first published online : 18 SEP 2002, DOI: 10.1002/ajmg.a.10914

  7. Fragmentariske studier over Bright'ske sygdomme, särlig over svulne, glatte, ikkeamyloide nyrer.

    Nordiskt Medicinskt Arkiv

    Volume 13, Issue 11, January/December 1881, Pages: 1–47, Overläge Dr med EDVARD BULL

    Article first published online : 24 APR 2009, DOI: 10.1111/j.0954-6820.1881.tb01230.x

  8. No evidence for submicroscopic 22qter deletions in patients with features suggestive for Angelman syndrome

    American Journal of Medical Genetics

    Volume 109, Issue 2, 22 April 2002, Pages: 117–120, Bert BA de Vries, Jess Tyson, Robin M Winter and Sue Malcolm

    Article first published online : 15 MAR 2002, DOI: 10.1002/ajmg.10318

  9. Kousseff syndrome caused by deletion of chromosome 22q11-13

    American Journal of Medical Genetics

    Volume 112, Issue 4, 1 November 2002, Pages: 338–342, Shawnia Forrester, Margaret J. Kovach, Randell E. Smith, Lisa Rimer, Melissa Wesson and Virginia E. Kimonis

    Article first published online : 8 JUL 2002, DOI: 10.1002/ajmg.10625

  10. 22q13 deletion syndrome

    American Journal of Medical Genetics

    Volume 101, Issue 2, 15 June 2001, Pages: 91–99, Mary C. Phelan, R. Curtis Rogers, Robert A. Saul, Gail A. Stapleton, Kevin Sweet, Heather McDermid, Steven R. Shaw, Joanne Claytor, Jan Willis and Desmond P. Kelly

    Article first published online : 29 MAY 2001, DOI: 10.1002/1096-8628(20010615)101:2<91::AID-AJMG1340>3.0.CO;2-C

  11. Minute supernumerary marker chromosomes identified in two patients with a related, larger pseudodicentric chromosome

    American Journal of Medical Genetics

    Volume 103, Issue 3, 15 October 2001, Pages: 193–197, Gloria Tung, Susan M. Covert, Katherine L. Malabed, Monica M. Wohlferd, Karen P. Beckerman, James D. Goldberg and Philip D. Cotter

    Article first published online : 30 AUG 2001, DOI: 10.1002/ajmg.1565

  12. Om kombinerte Bright'ske sygdomme

    Nordiskt Medicinskt Arkiv

    Volume 11, Issue 28, January/December 1879, Pages: 1–52, Dr. med. EDVAED BULL

    Article first published online : 24 APR 2009, DOI: 10.1111/j.0954-6820.1879.tb01105.x

  13. Assessment and management of hypertension in patients with type 2 diabetes

    Internal Medicine Journal

    Volume 39, Issue 3, March 2009, Pages: 143–149, M. C. Thomas and 1,2 R. Atkins 2

    Article first published online : 2 SEP 2008, DOI: 10.1111/j.1445-5994.2008.01696.x

  14. You have free access to this content
    Fine mapping of chromosome 22q tumor suppressor gene candidate regions in astrocytoma

    International Journal of Cancer

    Volume 108, Issue 6, 1 March 2004, Pages: 839–844, Christian Hartmann, Astrid Nümann, Wolf Mueller, Nikola Holtkamp, Matthias Simon and Andreas von Deimling

    Article first published online : 20 NOV 2003, DOI: 10.1002/ijc.11638

  15. Bernard-Soulier syndrome associated with 22q11.2 microdeletion

    American Journal of Medical Genetics

    Volume 99, Issue 4, 1 April 2001, Pages: 286–288, Masao Nakagawa, Masahiko Okuno, Nobuhiko Okamoto, Hidetoshi Fujino and Hirofumi Kato

    Article first published online : 21 FEB 2001, DOI: 10.1002/1096-8628(2001)9999:9999<::AID-AJMG1176>3.0.CO;2-T

  16. Complex chromosome 22 rearrangements in astrocytic tumors identified using microsatellite and chromosome 22 tile path array analysis

    Genes, Chromosomes and Cancer

    Volume 43, Issue 2, June 2005, Pages: 181–193, Tzer Jing Seng, Koichi Ichimura, Lu Liu, Ola Tingby, Danita M. Pearson and V. Peter Collins

    Article first published online : 15 MAR 2005, DOI: 10.1002/gcc.20181

  17. Defining a common region of DNA amplification at 22q11.2–12 in head and neck squamous cell carcinomas by quantitative FISH analysis

    Genes, Chromosomes and Cancer

    Volume 29, Issue 3, November 2000, Pages: 207–212, Kouji Matsumura, Akio Iritani, Shoji Enomoto, Chikao Torikata, Shigeo Matsuyama, Akira Kurita, Hiroki Kurahashi and Nobuo Tsuchida

    Article first published online : 3 AUG 2000, DOI: 10.1002/1098-2264(2000)9999:9999<::AID-GCC1032>3.0.CO;2-U

  18. SKY™ assessment of two karyotypes with 0–6 supernumerary marker/ring chromosomes and review of previously reported cases with two or more markers

    American Journal of Medical Genetics Part A

    Volume 118A, Issue 2, 15 April 2003, Pages: 156–171, Kavita S. Reddy, Shirong Wang, Shannon Groh and John Gonatos

    Article first published online : 17 MAR 2003, DOI: 10.1002/ajmg.a.10045

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    Asymmetry: Molecular, biologic, embryopathic, and clinical perspectives

    American Journal of Medical Genetics

    Volume 101, Issue 4, 15 July 2001, Pages: 292–314, Dr. M. Michael Cohen Jr.

    Article first published online : 8 JUN 2001, DOI: 10.1002/ajmg.1217

  20. Om den parenkymatösa nefritens förekomst i den späda barnaåldern såsom komplikation till andra sjukdomar, med särskildt afseende fästadt på dess närvaro vid tarmkatarr

    Nordiskt Medicinskt Arkiv

    Volume 1, Issue 16, January/December 1869, Pages: 1–42, Dr. ADOLF KJELLBERG

    Article first published online : 24 APR 2009, DOI: 10.1111/j.0954-6820.1869.tb00012.x