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There are 8568 results for: content related to: Familial Temporal Lobe Epilepsy with Aphasic Seizures and Linkage to Chromosome 10q22-q24

  1. Search for a shared segment on chromosome 10q26 in patients with bipolar affective disorder or schizophrenia from the Faroe Islands

    American Journal of Medical Genetics

    Volume 114, Issue 2, 8 March 2002, Pages: 196–204, Henrik Ewald, Tracey J. Flint, Tove H. Jorgensen, August G. Wang, Per Jensen, Maria Vang, Ole Mors and Torben A. Kruse

    Version of Record online : 7 FEB 2002, DOI: 10.1002/ajmg.10148

  2. Limitations of stratifying sib-pair data in common disease linkage studies: An example using chromosome 10p14-10q11 in type 1 diabetes

    American Journal of Medical Genetics

    Volume 113, Issue 2, 22 November 2002, Pages: 158–166, Gillian C.L. Johnson, Bobby P.C. Koeleman and John A. Todd

    Version of Record online : 25 SEP 2002, DOI: 10.1002/ajmg.10737

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    Microsatellite analysis at 10q25-q26 in Sardinian patients with sporadic endometrial carcinoma

    Cancer

    Volume 89, Issue 8, 15 October 2000, Pages: 1773–1782, Giuseppe Palmieri, Antonella Manca, Antonio Cossu, Giovanni Ruiu, Marina Pisano, PierLuigi Cherchi, Salvatore Dessole, Adriana Pintus, Giovannino Massarelli, Francesco Tanda and Mario Pirastu

    Version of Record online : 13 NOV 2000, DOI: 10.1002/1097-0142(20001015)89:8<1773::AID-CNCR18>3.0.CO;2-H

  4. Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33–q26.13 in Arab Israeli families

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 7, 5 October 2009, Pages: 914–925, A. Alkelai, Y. Kohn, T. Olender, K. Sarner-Kanyas, A. Rigbi, A. Hamdan, E. Ben-Asher, D. Lancet and B. Lerer

    Version of Record online : 16 JAN 2009, DOI: 10.1002/ajmg.b.30918

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    Molecular Genetics of Late-Onset Alzheimer's Disease

    Annals of Human Genetics

    Volume 68, Issue 4, July 2004, Pages: 381–404, M. Ilyas Kamboh

    Version of Record online : 28 JUN 2004, DOI: 10.1046/j.1529-8817.2004.00110.x

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    Epistasis Between Type 2 Diabetes Susceptibility Loci on Chromosomes 1q21-25 and 10q23-26 in Northern Europeans

    Annals of Human Genetics

    Volume 70, Issue 6, November 2006, Pages: 726–737, S. Wiltshire, J. T. Bell, C. J. Groves, C. Dina, A. T. Hattersley, T. M. Frayling, M. Walker, G. A. Hitman, M. Vaxillaire, M. Farrall, P. Froguel and M. I. McCarthy

    Version of Record online : 31 MAR 2006, DOI: 10.1111/j.1469-1809.2006.00289.x

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    Loss of heterozygosity on chromosome 10q is associated with earlier onset sporadic colorectal adenocarcinoma

    International Journal of Cancer

    Volume 99, Issue 6, 20 June 2002, Pages: 829–833, Adeshina S. Fawole, David J. Simpson, Ramesh Rajagopal, Jackie Elder, Tracey A. Holland, Anthony Fryer, Mark Deakin, James B. Elder and William E. Farrell

    Version of Record online : 24 APR 2002, DOI: 10.1002/ijc.10432

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    KLF6, a putative tumor suppressor gene, is mutated in astrocytic gliomas

    International Journal of Cancer

    Volume 105, Issue 5, 10 July 2003, Pages: 625–629, Yung-Ming Jeng and Hey-Chi Hsu

    Version of Record online : 25 MAR 2003, DOI: 10.1002/ijc.11123

  9. Genetic fine mapping of the gene for nonsyndromic congenital retinal nonattachment

    American Journal of Medical Genetics

    Volume 92, Issue 3, 29 May 2000, Pages: 220–223, N.M. Ghiasvand, T.P. Fleming, C. Helms, Aledavood Avisa and H. Donis-Keller

    Version of Record online : 22 MAY 2000, DOI: 10.1002/(SICI)1096-8628(20000529)92:3<220::AID-AJMG11>3.0.CO;2-Y

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    Loss of heterozygosity at 10q in tumors of the upper respiratory tract is associated with poor prognosis

    International Journal of Cancer

    Volume 84, Issue 4, 20 August 1999, Pages: 432–436, Daniela Gasparotto, Tamara Vukosavljevic, Sara Piccinin, Luigi Barzan, Sandro Sulfaro, Michela Armellin, Mauro Boiocchi and Roberta Maestro

    Version of Record online : 10 NOV 1999, DOI: 10.1002/(SICI)1097-0215(19990820)84:4<432::AID-IJC18>3.0.CO;2-#

  11. A locus for generalized tonic-clonic seizure susceptibility maps to chromosome 10q25-q26

    Annals of Neurology

    Volume 58, Issue 3, September 2005, Pages: 449–458, Ram S. Puranam, Satish Jain, Amber M. Kleindienst, Shilpa Saxena, Myeong-Kyu Kim, Barbara Kelly Changizi, M. V. Padma, Ian Andrews, Robert C. Elston, Hemant K. Tiwari and James O. McNamara

    Version of Record online : 29 AUG 2005, DOI: 10.1002/ana.20598

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    Evidence for a Type 1 Diabetes Susceptibility Locus (IDDM10) on Chromosome 10p11-q11 in a Russian Population

    Scandinavian Journal of Immunology

    Volume 60, Issue 3, September 2004, Pages: 316–323, D. A. Chistiakov, Y. Seryogin, K. V. Savost'anov, L. I. Zilberman, E. V. Titovich, T. L. Kuraeva, I. I. Dedov and V. V. Nosikov

    Version of Record online : 20 AUG 2004, DOI: 10.1111/j.0300-9475.2004.01480.x

  13. Genome-scan for loci involved in cleft lip with or without cleft palate in consanguineous families from Turkey

    American Journal of Medical Genetics Part A

    Volume 126A, Issue 2, 15 April 2004, Pages: 111–122, Mary L. Marazita, L. Leigh Field, Gökhan Tunçbilek, Margaret E. Cooper, Toby Goldstein and K. Gürler Gürsu

    Version of Record online : 24 OCT 2003, DOI: 10.1002/ajmg.a.20564

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    Four New Families with Autosomal Dominant Partial Epilepsy with Auditory Features: Clinical Description and Linkage to Chromosome 10q24

    Epilepsia

    Volume 43, Issue 1, January 2002, Pages: 60–67, Melodie R. Winawer, Filippo Martinelli Boneschi, Christie Barker-Cummings, Joseph H. Lee, Jianjun Liu, Constantine Mekios, T. Conrad Gilliam, Timothy A. Pedley, W. Allen Hauser and Ruth Ottman

    Version of Record online : 2 APR 2002, DOI: 10.1046/j.1528-1157.2002.45001.x

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    Refinement of the adPEO linked locus on Chr10 and analysis of MRS4 and three other candidate genes

    FEBS Letters

    Volume 500, Issue 3, July 06, 2001, Pages: 183–185, Sharon Lewis, Wendy Hutchison, Lisa Di Nezza, Dominic Thyagarajan, Rosetta Marotta and Henrik Dahl

    Version of Record online : 2 JUL 2001, DOI: 10.1016/S0014-5793(01)02612-6

  16. A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 5, 1 March 2008, Pages: 578–584, Peter Kinirons, Dominique J. Verlaan, Marie-Pierre Dubé, Josée Poirier, Charles Deacon, Anne Lortie, Jean-François Clément, Richard Desbiens, Lionel Carmant, Cecile Cieuta-Walti, Michael Shevell, Guy A. Rouleau and Patrick Cossette

    Version of Record online : 1 FEB 2008, DOI: 10.1002/ajmg.a.32139

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    Characterization of 26 MiniSTR Loci for Improved Analysis of Degraded DNA Samples

    Journal of Forensic Sciences

    Volume 53, Issue 1, January 2008, Pages: 73–80, Carolyn R. Hill, Margaret C. Kline, Michael D. Coble and John M. Butler

    Version of Record online : 14 NOV 2007, DOI: 10.1111/j.1556-4029.2008.00595.x

  18. Genome wide scan using homozygosity mapping and linkage analyses of a single pedigree with affective disorder suggests oligogenic inheritance

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 120B, Issue 1, 1 July 2003, Pages: 63–71, Henrik Ewald, Torben A. Kruse and Ole Mors

    Version of Record online : 10 APR 2003, DOI: 10.1002/ajmg.b.20039

  19. Chromosome 10q24.3-qter deletion associated with left-sided first branchial arch defect, diaphragmatic eventration, and duplicated renal pelvis

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 20, 15 October 2006, Pages: 2241–2244, Jia-Woei Hou

    Version of Record online : 12 SEP 2006, DOI: 10.1002/ajmg.a.31429

  20. Genetic heterogeneity in inherited spastic paraplegia associated with epilepsy

    American Journal of Medical Genetics Part A

    Volume 117A, Issue 2, 1 March 2003, Pages: 116–121, Cristiana Lo Nigro, Roberto Cusano, Gian Luigi Gigli, Paola Forabosco, Mariarosaria Valente, Roberto Ravazzolo, Marina Diomedi and Marco Seri

    Version of Record online : 13 JAN 2003, DOI: 10.1002/ajmg.a.10141