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There are 46587 results for: content related to: Genetic mapping using haplotype and model-free linkage analysis supports previous evidence for a locus predisposing to severe bipolar disorder at 5q31-33

  1. Integration of genetic maps by polynomial transformations

    American Journal of Medical Genetics

    Volume 96, Issue 1, 7 February 2000, Pages: 108–113, H.H. Stassen and C. Scharfetter

    Version of Record online : 23 FEB 2000, DOI: 10.1002/(SICI)1096-8628(20000207)96:1<108::AID-AJMG21>3.0.CO;2-J

  2. Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on chromosome 5qter

    American Journal of Medical Genetics

    Volume 104, Issue 2, 22 November 2001, Pages: 152–156, Meital Gal Tanamy, Nurit Magal, Gabrielle J. Halpern, Lutfi Jaber and Mordechai Shohat

    Version of Record online : 5 NOV 2002, DOI: 10.1002/ajmg.10030

  3. Fine mapping study in Scandinavian families suggests association between coeliac disease and haplotypes in chromosome region 5q32

    Tissue Antigens

    Volume 71, Issue 1, January 2008, Pages: 27–34, S. Adamovic, S. S. Amundsen, B. A. Lie, Å. Hellqvist, A. H. Gudjónsdóttir, J. Ek, S. Nilsson, J. Wahlström, H. Ascher, L. M. Sollid and Å. T. Naluai

    Version of Record online : 30 OCT 2007, DOI: 10.1111/j.1399-0039.2007.00955.x

  4. You have free access to this content
    Distinct regions of frequent loss of heterozygosity of chromosome 5p and 5q in human esophageal cancer

    International Journal of Cancer

    Volume 78, Issue 5, 23 November 1998, Pages: 600–605, Robert C. Peralta, Alan G. Casson, Rui-nan Wang, Shaf Keshavjee, Mark Redston and Bharati Bapat

    Version of Record online : 12 DEC 1998, DOI: 10.1002/(SICI)1097-0215(19981123)78:5<600::AID-IJC12>3.0.CO;2-1

  5. You have free access to this content
    Duplication of two distinct regions on chromosome 5Q in non-papillary renal-cell carcinomas

    International Journal of Cancer

    Volume 76, Issue 3, 4 May 1998, Pages: 337–340, Peter Bugert, Rolf Von Knobloch and Gyula Kovacs

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1097-0215(19980504)76:3<337::AID-IJC9>3.0.CO;2-W

  6. Exploring the dense mapping of a region of potential linkage in complex disease: An example in multiple sclerosis

    Genetic Epidemiology

    Volume 17, Issue 1, 1999, Pages: 51–63, Robert Feakes, Stephen Sawcer, Jeremy Chataway, Francesca Coraddu, Simon Broadley, Julia Gray, Hywel B. Jones, David Clayton, Peter N. Goodfellow and Alastair Compston

    Version of Record online : 21 APR 1999, DOI: 10.1002/(SICI)1098-2272(1999)17:1<51::AID-GEPI4>3.0.CO;2-V

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    New DNA markers with increased informativeness show diminished support for a chromosome 5q11–13 schizophrenia susceptibility locus and exclude linkage in two new cohorts of British and Icelandic families

    Annals of Human Genetics

    Volume 63, Issue 3, May 1999, Pages: 235–247, G. KALSI, B. MANKOO, D. CURTIS, R. SHERRINGTON, G. MELMER, J. BRYNJOLFSSON, T. SIGMUNDSSON, T. READ, P. MURPHY, H. PETURSSON and H. GURLING

    Version of Record online : 4 MAR 2003, DOI: 10.1046/j.1469-1809.1999.6330235.x

  8. Report of the Chromosome 5 Workshop of the Sixth World Congress on Psychiatric Genetics

    American Journal of Medical Genetics

    Volume 88, Issue 3, 18 June 1999, Pages: 229–232, Raymond R. Crowe, Veronica Vieland, S.D. Detera-Wadleigh, D.L. Garver, P.V. Gejman, I. Hovatta and E. Shink

    Version of Record online : 10 MAY 1999, DOI: 10.1002/(SICI)1096-8628(19990618)88:3<229::AID-AJMG4>3.0.CO;2-B

  9. A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 7, 5 October 2009, Pages: 998–1006, A.J. Jasinska, S. Service, D. Jawaheer, J. DeYoung, M. Levinson, Z. Zhang, B. Kremeyer, H. Muller, I. Aldana, J. Garcia, G. Restrepo, C. Lopez, C. Palacio, C. Duque, M. Parra, J. Vega, D. Ortiz, G. Bedoya, C. Mathews, P. Davanzo, E. Fournier, J. Bejarano, M. Ramirez, C. Araya Ortiz, X. Araya, J. Molina, C. Sabatti, V. Reus, J. Ospina, G. Macaya, A. Ruiz-Linares and N.B. Freimer

    Version of Record online : 24 MAR 2009, DOI: 10.1002/ajmg.b.30956

  10. Evidence of a locus for schizophrenia and related disorders on the short arm of chromosome 5 in a large pedigree

    American Journal of Medical Genetics

    Volume 67, Issue 2, 9 April 1996, Pages: 162–171, Jeremy M. Silverman, David A. Greenberg, Larry D. Altstiel, Larry J. Siever, Richard C. Mohs, Christopher J. Smith, Guilan Zhou, Tovah E. Hollander, Xin-Ping Yang, Medhi Kedache, Ge Li, Michele L. Zaccario and Kenneth L. Davis

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19960409)67:2<162::AID-AJMG6>3.0.CO;2-U

  11. Linkage disequlibrium in the DTNBP1 (dysbindin) gene region and on chromosome 1p36 among psychotic patients from a genetic isolate in Israel: Findings from identity by descent haplotype sharing analysis

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 128B, Issue 1, 1 July 2004, Pages: 65–70, Yoav Kohn, Eduardo Danilovich, Dvorah Filon, Ariella Oppenheim, Osnat Karni, Kyra Kanyas, Neil Turetsky, Mira Korner and Bernard Lerer

    Version of Record online : 20 MAY 2004, DOI: 10.1002/ajmg.b.30044

  12. Apparent genetic homogeneity of the treacher Collins-Franceschetti syndrome

    American Journal of Medical Genetics

    Volume 52, Issue 2, 15 August 1994, Pages: 174–177, Patrick Edery, Yves Manach, Martine Le Merrer, Marianne Till, Alain Vignal, Stanislas Lyonnet and Arnold Munnich

    Version of Record online : 7 JUN 2005, DOI: 10.1002/ajmg.1320520210

  13. Fortuitous FISH diagnosis of an interstitial microdeletion (5)(q31.1q31.2) in a girl suspected to present a cri-du-chat syndrome

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 12, 15 June 2007, Pages: 1342–1347, A.L. Mosca, P. Callier, B. Leheup, N. Marle, M. Jalloul, L. Coffinet, F. Feillet, M. Valduga, P. Jonveaux and F. Mugneret

    Version of Record online : 15 MAY 2007, DOI: 10.1002/ajmg.a.31742

  14. Genetic mapping of a novel familial form of infantile hemangioma

    American Journal of Medical Genetics

    Volume 82, Issue 1, 1 January 1999, Pages: 77–83, Jeffrey W. Walter, Francine Blei, Jennifer L. Anderson, Seth J. Orlow, Marcy C. Speer and Douglas A. Marchuk

    Version of Record online : 29 JAN 1999, DOI: 10.1002/(SICI)1096-8628(19990101)82:1<77::AID-AJMG15>3.0.CO;2-A

  15. Characterization of an unbalanced de novo rearrangement by microsatellite polymorphism typing and by fluorescent in situ hybridization

    American Journal of Medical Genetics

    Volume 56, Issue 4, 8 May 1995, Pages: 398–402, Jian Zhao, Patricia L. Gordon, R. Sid Wilroy Jr., Paula R. Martens, Jack Tarleton, Lee P. Shulman, Joe Leigh Simpson, Sherman Elias and Avirachan T. Tharapel

    Version of Record online : 7 JUN 2005, DOI: 10.1002/ajmg.1320560410

  16. You have full text access to this OnlineOpen article
    DIP–STR: Highly Sensitive Markers for the Analysis of Unbalanced Genomic Mixtures

    Human Mutation

    Volume 34, Issue 4, April 2013, Pages: 644–654, Vincent Castella, Joëlle Gervaix and Diana Hall

    Version of Record online : 5 MAR 2013, DOI: 10.1002/humu.22280

  17. Chromosome 5 and Gilles de la Tourette syndrome: Linkage in a large pedigree and association study of six candidates in the region

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 1, 5 January 2009, Pages: 95–103, Nancy Laurin, Karen G. Wigg, Yu Feng, Paul Sandor and Cathy L. Barr

    Version of Record online : 2 MAY 2008, DOI: 10.1002/ajmg.b.30779

  18. High resolution genetic map of the adenomatous polyposis coli gene (APC) region

    American Journal of Medical Genetics

    Volume 56, Issue 4, 8 May 1995, Pages: 413–419, Sylviane Olschwang, Pierre Laurent-Puig, Thomas Melot, Bénédicte Thuille and Dr. Gilles Thomas

    Version of Record online : 3 JUN 2005, DOI: 10.1002/ajmg.1320560413

  19. Genome-wide search for linkage of bipolar affective disorders in a very large pedigree derived from a homogeneous population in Quebec points to a locus of major effect on chromosome 12q23 q24

    American Journal of Medical Genetics

    Volume 88, Issue 5, 15 October 1999, Pages: 567–587, J. Morissette, A. Villeneuve, L. Bordeleau, D. Rochette, C. Laberge, B. Gagné, C. Laprise, G. Bouchard, M. Plante, L. Gobeil, E. Shink, J. Weissenbach and N. Barden

    Version of Record online : 17 SEP 1999, DOI: 10.1002/(SICI)1096-8628(19991015)88:5<567::AID-AJMG24>3.0.CO;2-8

  20. Adult-onset autosomal dominant leukodystrophy with autonomic symptoms restricted to 1.5 Mbp on chromosome 5q23

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 141B, Issue 6, 5 September 2006, Pages: 608–614, Lena Marklund, Malin Melin, Atle Melberg, Vilmantas Giedraitis and Niklas Dahl

    Version of Record online : 5 JUL 2006, DOI: 10.1002/ajmg.b.30342