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There are 56816 results for: content related to: Defining the autism minimum candidate gene region on chromosome 7

  1. 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

    Article first published online : 6 FEB 2006, DOI: 10.1002/ajmg.a.31110

  2. Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: Clinical report and review

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 8, 15 April 2007, Pages: 791–798, P.A. Lennon, M.L. Cooper, D.A. Peiffer, K.L. Gunderson, A. Patel, Sarika Peters, S.W. Cheung and C.A. Bacino

    Article first published online : 1 MAR 2007, DOI: 10.1002/ajmg.a.31632

  3. Incorporating language phenotypes strengthens evidence of linkage to autism

    American Journal of Medical Genetics

    Volume 105, Issue 6, 8 August 2001, Pages: 539–547, Yuki Bradford, Jonathan Haines, Holli Hutcheson, Marybeth Gardiner, Terry Braun, Val Sheffield, Tom Cassavant, Wen Huang, Kai Wang, Veronica Vieland, Susan Folstein, Susan Santangelo and Joseph Piven

    Article first published online : 6 JUL 2001, DOI: 10.1002/ajmg.1497

  4. 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

    Article first published online : 9 JAN 2003, DOI: 10.1002/ajmg.a.10209

  5. 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

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

  6. Familial cerebral cavernous angioma: A gene localized to a 15-cm interval on chromosome 7q

    Annals of Neurology

    Volume 39, Issue 6, June 1996, Pages: 807–810, A. Gil-Nagel, J. Dubovsky, K. J. Wilcox, J. M. Stewart, V. E Anderson, I. E Leppik, H. T Orr, E. W Johnson, J. L. Weber and S. S. Rich

    Article first published online : 8 OCT 2004, DOI: 10.1002/ana.410390619

  7. A study of linkage and association of body mass index in the old order Amish

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

    Volume 121C, Issue 1, 15 August 2003, Pages: 71–80, P. Platte, G.J. Papanicolaou, J. Johnston, C.M. Klein, K.F. Doheny, E.W. Pugh, M.-H. Roy-Gagnon, A.J. Stunkard, C.A. Francomano and A.F. Wilson

    Article first published online : 26 JUN 2003, DOI: 10.1002/ajmg.c.20005

  8. Genetic linkage mapping for a susceptibility locus to bipolar illness: Chromosomes 2,3,4,7,9,10p,11p,22, and Xpter

    American Journal of Medical Genetics

    Volume 54, Issue 3, 15 September 1994, Pages: 206–218, Sevilla D. Detera-Wadleigh, Wang-Ting Hsieh, Wade H. Berrettini, Lynn R. Goldin, Denise Y. Rollins, David Muniec, Raji Grewal, Juliet J. Guroff, Gordon Turner, Diane Coffman, J. Barrick, Kate Mills, Jeffrey Murray, Susan J. Donohue, David C. Klein, Jason Sanders, John I. Nurnberger Jr. and Elliot S. Gershon

    Article first published online : 7 JUN 2005, DOI: 10.1002/ajmg.1320540307

  9. Evidence supporting WNT2 as an autism susceptibility gene

    American Journal of Medical Genetics

    Volume 105, Issue 5, 8 July 2001, Pages: 406–413, Thomas H. Wassink, Joseph Piven, Veronica J. Vieland, Jian Huang, Ruth E. Swiderski, Jennifer Pietila, Terry Braun, Gretel Beck, Susan E. Folstein, Jonathon L. Haines and Val C. Sheffield

    Article first published online : 17 MAY 2001, DOI: 10.1002/ajmg.1401

  10. Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31

    American Journal of Medical Genetics

    Volume 78, Issue 2, 30 June 1998, Pages: 107–113, John H. Greinwald Jr., Sigrid Wayne, Achih H. Chen, Daryl A. Scott, Ross I.S. Zbar, Michelle L. Kraft, Sai Prasad, Arabandi Ramesh, Paul Coucke, C.R. Srikumari Srisailapathy, Michael Lovett, Guy Van Camp and Richard J.H. Smith

    Article first published online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19980630)78:2<107::AID-AJMG2>3.0.CO;2-L

  11. Molecular cytogenetic characterization of del(7q) in two uterine leiomyoma-derived cell lines

    Genes, Chromosomes and Cancer

    Volume 18, Issue 3, March 1997, Pages: 155–161, Roberta Vanni, Susanna Marras, Eric F. P. M. Schoenmakers, Paola Dal Cin, Bernd Kazmierczak, Gabriele Senger, Jörn Bullerdiek, Wim J. M. Van de Ven and Herman Van den Berghe

    Article first published online : 7 DEC 1998, DOI: 10.1002/(SICI)1098-2264(199703)18:3<155::AID-GCC1>3.0.CO;2-0

  12. Frequent deletions within FRA7G at 7q31.2 in invasive epithelial ovarian cancer

    Genes, Chromosomes and Cancer

    Volume 24, Issue 1, January 1999, Pages: 48–55, Haojie Huang, Christopher P. Reed, Aderonke Mordi, Gwen Lomberk, Liang Wang, Viji Shridhar, Lynn Hartmann, Robert Jenkins and David I. Smith

    Article first published online : 6 JAN 1999, DOI: 10.1002/(SICI)1098-2264(199901)24:1<48::AID-GCC7>3.0.CO;2-V

  13. Absracts

    Vox Sanguinis

    Volume 83, Issue S2, August 2002, Pages: 1–236,

    Article first published online : 9 AUG 2011, DOI: 10.1111/j.1423-0410.2002.tb05391.x

  14. You have full text access to this Open Access content
    Frequent Allelic Loss at 7p14-15 Associated with Aggressive Histologic Types of Breast Cancer

    Japanese Journal of Cancer Research

    Volume 89, Issue 5, May 1998, Pages: 533–538, Keisuke Kurose, Aritoshi Iida, Tsutomu Araki, Goi Sakamoto, Fujio Kasumi, Yusuke Nakamura and Mitsuru Emi

    Article first published online : 23 AUG 2005, DOI: 10.1111/j.1349-7006.1998.tb03294.x

  15. Length and sequence variation in D7S22 (g3) alleles studied by high resolution length measurements and nucleotide sequencing


    Volume 18, Issue 5, 1997, Pages: 675–681, Rune Andreassen and Bjørnar Olaisen

    Article first published online : 14 APR 2005, DOI: 10.1002/elps.1150180503

  16. Association between 7q31 markers and tourette syndrome

    American Journal of Medical Genetics Part A

    Volume 127A, Issue 1, 15 May 2004, Pages: 17–20, Adriana Díaz-Anzaldúa, Ridha Joober, Jean-Baptiste Rivière, Yves Dion, Paul Lespérance, Sylvain Chouinard, Francois Richer and Guy Armand Rouleau

    Article first published online : 17 DEC 2003, DOI: 10.1002/ajmg.a.20631

  17. Linkage of preaxial polydactyly type 2 to 7q36

    American Journal of Medical Genetics

    Volume 58, Issue 2, 28 August 1995, Pages: 128–135, Anne V. Hing, Cynthia Helms, Rachel Slaugh, Andrea Burgess, Jen C. Wang, Thomas Herman, S. Bruce Dowton and Helen Donis-Keller

    Article first published online : 16 MAY 2005, DOI: 10.1002/ajmg.1320580208

  18. Use of phytochemomics to evaluate the bioavailability and bioactivity of antioxidant peptides of soybean β-conglycinin


    Volume 35, Issue 11, June 2014, Pages: 1582–1589, Miryam Amigo-Benavent, Alfonso Clemente, Simonetta Caira, Paola Stiuso, Pasquale Ferranti and M. Dolores del Castillo

    Article first published online : 7 FEB 2014, DOI: 10.1002/elps.201300527

  19. Elucidation of a cryptic interstitial 7q31.3 deletion in a patient with a language disorder and mild mental retardation by array-CGH

    American Journal of Medical Genetics Part A

    Volume 129A, Issue 3, 1 September 2004, Pages: 254–260, Christine Tyson, Barbara McGillivray, Chieko Chijiwa and Evica Rajcan-Separovic

    Article first published online : 21 JUL 2004, DOI: 10.1002/ajmg.a.30245

  20. Germline mutations of the POU6F2 gene in Wilms tumors with loss of heterozygosity on chromosome 7p14

    Human Mutation

    Volume 24, Issue 5, November 2004, Pages: 400–407, Daniela Perotti, Giovanna De Vecchi, Maria A. Testi, Elena Lualdi, Piergiorgio Modena, Patrizia Mondini, Fernando Ravagnani, Paola Collini, Francesca Di Renzo, Filippo Spreafico, Monica Terenziani, Gabriella Sozzi, Franca Fossati-Bellani and Paolo Radice

    Article first published online : 30 SEP 2004, DOI: 10.1002/humu.20096