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There are 7818 results for: content related to: Incorporating language phenotypes strengthens evidence of linkage to autism

  1. You have free access to this content
    The Human Obesity Gene Map: The 2004 Update

    Obesity Research

    Volume 13, Issue 3, March 2005, Pages: 381–490, Louis Pérusse, Tuomo Rankinen, Aamir Zuberi, Yvon C. Chagnon, S. John Weisnagel, George Argyropoulos, Brandon Walts, Eric E. Snyder and Claude Bouchard

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2005.50

  2. Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7q

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 156, Issue 2, March 2011, Pages: 168–176, Haiyan Xu, Rong Cheng, Suh-Hang Juo, Jianjun Liu, Jo Ellen Loth, Jean Endicott, Conrad Gilliam and Miron Baron

    Version of Record online : 16 DEC 2010, DOI: 10.1002/ajmg.b.31151

  3. 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

  4. You have free access to this content
    The Human Obesity Gene Map: The 2003 Update

    Obesity Research

    Volume 12, Issue 3, March 2004, Pages: 369–439, Eric E. Snyder, Brandon Walts, Louis Pérusse, Yvon C. Chagnon, S. John Weisnagel, Tuomo Rankinen and Claude Bouchard

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2004.47

  5. Fine mapping supports previous linkage evidence for a bipolar disorder susceptibility locus on 13q32

    American Journal of Medical Genetics

    Volume 105, Issue 4, 8 May 2001, Pages: 375–380, Chunyu Liu, Judith A. Badner, Susan L. Christian, Juliet J. Guroff, Sevilla D. Detera-Wadleigh and Elliot S. Gershon

    Version of Record online : 30 APR 2001, DOI: 10.1002/ajmg.1358

  6. Concordance Study Between the AmpFℓSTR® MiniFilerTM PCR Amplification Kit and Conventional STR Typing Kits

    Journal of Forensic Sciences

    Volume 52, Issue 4, July 2007, Pages: 870–873, Carolyn R. Hill, Margaret C. Kline, Julio J. Mulero, Robert E. Lagacé, Chien-Wei Chang, Lori K. Hennessy and John M. Butler

    Version of Record online : 6 JUN 2007, DOI: 10.1111/j.1556-4029.2007.00491.x

  7. Autosomal Short Tandem Repeat Analysis of Ancient DNA by Coupled Use of Mini- and Conventional STR Kits

    Journal of Forensic Sciences

    Volume 57, Issue 3, May 2012, Pages: 820–825, Chang Seok Oh, Sang Jun Lee, Jun Bum Park, Soong Deok Lee, Seung Bum Seo, Hye Yeon Kim, Jaehyup Kim, Yi-Suk Kim and Dong Hoon Shin

    Version of Record online : 23 JAN 2012, DOI: 10.1111/j.1556-4029.2011.02044.x

  8. Further evidence for linkage of bipolar disorder to chromosomes 6 and 17 in a new independent pedigree series

    Bipolar Disorders

    Volume 14, Issue 1, February 2012, Pages: 71–79, Tiffany A Greenwood, Caroline M Nievergelt, A Dessa Sadovnick, Ronald A Remick, Paul E Keck Jr, Susan L McElroy, Tatyana Shekhtman, Rebecca McKinney and John R Kelsoe

    Version of Record online : 13 FEB 2012, DOI: 10.1111/j.1399-5618.2011.00970.x

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    Genes encoding human caveolin-1 and -2 are co-localized to the D7S522 locus (7q31.1), a known fragile site (FRA7G) that is frequently deleted in human cancers

    FEBS Letters

    Volume 436, Issue 3, October 09, 1998, Pages: 403–410, Jeffrey A Engelman, Xiao Lan Zhang and Michael P Lisanti

    Version of Record online : 23 OCT 1998, DOI: 10.1016/S0014-5793(98)01134-X

  10. A genome wide search for alcoholism susceptibility genes

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 128B, Issue 1, 1 July 2004, Pages: 102–113, Shirley Y. Hill, Sa Shen, Nicholas Zezza, Eric K. Hoffman, Mark Perlin and William Allan

    Version of Record online : 9 MAR 2004, DOI: 10.1002/ajmg.b.30013

  11. Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 5, 1 March 2006, Pages: 509–514, Susan Zeesman, Małgorzata J.M. Nowaczyk, Ikuko Teshima, Wendy Roberts, Janis Oram Cardy, Jessica Brian, Lili Senman, Lars Feuk, Lucy R. Osborne and Stephen W. Scherer

    Version of Record online : 6 FEB 2006, DOI: 10.1002/ajmg.a.31110

  12. Developmental Validation of Reduced-Size STR Miniplex Primer Sets

    Journal of Forensic Sciences

    Volume 52, Issue 6, November 2007, Pages: 1263–1271, Kerry L. Opel, Denise T. Chung, Jiří Drábek, John M. Butler and Bruce R. McCord

    Version of Record online : 10 DEC 2007, DOI: 10.1111/j.1556-4029.2007.00584.x

  13. Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11–q21.32

    Clinical Genetics

    Volume 72, Issue 1, July 2007, Pages: 23–29, A Wali, MS Chishti, M Ayub, M Yasinzai, , G Ali, P John and W Ahmad

    Version of Record online : 27 MAY 2007, DOI: 10.1111/j.1399-0004.2007.00818.x

  14. Developmental Validation of the AmpFℓSTR® Identifiler® Plus PCR Amplification Kit: An Established Multiplex Assay with Improved Performance

    Journal of Forensic Sciences

    Volume 57, Issue 2, March 2012, Pages: 453–465, Dennis Y. Wang, Chien-Wei Chang, Robert E. Lagacé, Lisa M. Calandro and Lori K. Hennessy

    Version of Record online : 10 NOV 2011, DOI: 10.1111/j.1556-4029.2011.01963.x

  15. Haplotype analysis of the growth hormone releasing hormone receptor locus in three apparently unrelated kindreds from the indian subcontinent with the identical mutation in the GHRH receptor

    American Journal of Medical Genetics Part A

    Volume 120A, Issue 1, 1 July 2003, Pages: 77–83, Michael P. Wajnrajch, Joseph M. Gertner, Alisa S. Sokoloff, Irina Ten, Madeleine D. Harbison, Irène Netchine, Hiralal G. Maheshwari, David B. Goldstein, Serge Amselem, Gerhard Baumann and Rudolph L. Leibel

    Version of Record online : 9 JAN 2003, DOI: 10.1002/ajmg.a.10209

  16. Allelotyping of esophageal squamous-cell carcinoma on chromosome 13 defines deletions related to family history

    Genes, Chromosomes and Cancer

    Volume 44, Issue 3, November 2005, Pages: 271–278, Nan Hu, Hua Su, Wen Jun Li, Carol Giffen, Alisa M. Goldstein, Ying Hu, Chaoyu Wang, Mark J Roth, Guang Li, Sanford M. Dawsey, Yi Xu, Philip R. Taylor and Michael R. Emmert-Buck

    Version of Record online : 13 JUL 2005, DOI: 10.1002/gcc.20242

  17. Two discrete regions of deletion at 7q in uterine leiomyomas

    Genes, Chromosomes and Cancer

    Volume 19, Issue 3, July 1997, Pages: 156–160, Chandramohan S. Ishwad, Robert E. Ferrell, Karen Hanley, Jayant Davare, Auvelia M. Meloni, Avery A. Sandberg and Urvashi Surti

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1098-2264(199707)19:3<156::AID-GCC4>3.0.CO;2-X

  18. Genetic signatures of pre-expansion bottleneck in the Choctaw population of Oklahoma

    American Journal of Physical Anthropology

    Volume 124, Issue 4, August 2004, Pages: 373–379, Ning Wang, Xiaodong Zhou, Filemon K. Tan, Morris W. Foster, Frank C. Arnett and Ranajit Chakraborty

    Version of Record online : 19 NOV 2003, DOI: 10.1002/ajpa.10363

  19. Genetics and Genomics of Core Short Tandem Repeat Loci Used in Human Identity Testing

    Journal of Forensic Sciences

    Volume 51, Issue 2, March 2006, Pages: 253–265, John M. Butler

    Version of Record online : 8 MAR 2006, DOI: 10.1111/j.1556-4029.2006.00046.x

  20. You have free access to this content
    The Human Obesity Gene Map: The 2002 Update

    Obesity Research

    Volume 11, Issue 3, March 2003, Pages: 313–367, Yvon C. Chagnon, Tuomo Rankinen, Eric E. Snyder, S. John Weisnagel, Louis Pérusse and Claude Bouchard

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2003.47