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There are 13708 results for: content related to: Park6-linked parkinsonism occurs in several european families

  1. Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset

    Annals of Neurology

    Volume 51, Issue 2, February 2002, Pages: 253–256, Vincenzo Bonifati, Guido J. Breedveld, Ferdinando Squitieri, Nicola Vanacore, Pierluigi Brustenghi, Biswadjiet S. Harhangi, Pasquale Montagna, Milena Cannella, Giovanni Fabbrini, Patrizia Rizzu, Cornelia M. van Duijn, Ben A. Oostra, Giuseppe Meco and Peter Heutink

    Article first published online : 31 JAN 2002, DOI: 10.1002/ana.10106

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    ARHI is the center of allelic deletion on chromosome 1p31 in ovarian and breast cancers

    International Journal of Cancer

    Volume 86, Issue 5, 1 June 2000, Pages: 690–694, Hongqi Peng, Fengji Xu, Rashmi Pershad, Kelly K. Hunt, Marsha L. Frazier, Andrew Berchuck, Joe W. Gray, David Hogg, Robert C. Bast Jr. and Yinhua Yu

    Article first published online : 27 APR 2000, DOI: 10.1002/(SICI)1097-0215(20000601)86:5<690::AID-IJC14>3.0.CO;2-K

  3. Current status of linkage studies in hereditary prostate cancer

    BJU International

    Volume 86, Issue 6, October 2000, Pages: 659–669, M.K. Karayi, D.E. Neal and A.F. Markham

    Article first published online : 24 DEC 2001, DOI: 10.1046/j.1464-410x.2000.00837.x

  4. Smallest region of overlapping deletion in 1p36 in human neuroblastoma: A 1 Mbp cosmid and PAC contig

    Genes, Chromosomes and Cancer

    Volume 31, Issue 3, July 2001, Pages: 228–239, Anja Bauer, Larissa Savelyeva, Andreas Claas, Christian Praml, Frank Berthold and Manfred Schwab

    Article first published online : 27 APR 2001, DOI: 10.1002/gcc.1139

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    Mapping the Gene Causing Hereditary Primary Hyperparathyroidism in a Portuguese Kindred to Chromosome 1q22-q31

    Journal of Bone and Mineral Research

    Volume 14, Issue 2, February 1999, Pages: 230–239, C. Williamson, B. M. Cavaco, A. Jauch, P. H. Dixon, S. Forbes, B. Harding, H. Holtgreve-Grez, B. Schoell, M. C. Pereira, A. P. Font, M. M. Loureiro, L. G. Sobrinho, M. A. Santos and Prof. R. V. Thakker

    Article first published online : 1 FEB 1999, DOI: 10.1359/jbmr.1999.14.2.230

  6. Linkage of schizophrenia with chromosome 1q32 in Korean multiplex families'

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 3, 5 April 2007, Pages: 279–284, Yong Lee Jang, Jong Won Kim, Yu-Sang Lee, Dong Yeon Park, Eun-Young Cho, Hyun Ok Jeun, Dongsoo Lee and Kyung Sue Hong

    Article first published online : 14 DEC 2006, DOI: 10.1002/ajmg.b.30389

  7. Genetic linkage and association between chromosome 1q and working memory function in schizophrenia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 116B, Issue 1, 1 January 2003, Pages: 8–16, Timothy L. Gasperoni, Jesper Ekelund, Matti Huttunen, Christina G.S. Palmer, Annamari Tuulio-Henriksson, Jouko Lönnqvist, Jaakko Kaprio, Leena Peltonen and Tyrone D. Cannon

    Article first published online : 14 OCT 2002, DOI: 10.1002/ajmg.b.10757

  8. Genome-scan for bipolar disorder with sib-pair families in the Sardinian population: A new susceptibility locus on chromosome 1p22–p21?

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 153B, Issue 6, September 2010, Pages: 1200–1208, Maria Del Zompo, Giovanni Severino, Raffaella Ardau, Caterina Chillotti, Mariapaola Piccardi, Colette Dib, Gaëlle Muzard, Stéphane Soubigou, Murielle Derock, Raphaël Fournel, Yves Vaubien, Sandrine Roche, Laurent Bowen-Squires, Emmanuelle Génin, Emmanuelle Cousin, Jean-François Deleuze, Nicole Faucon Biguet, Jacques Mallet and Rolando Meloni

    Article first published online : 12 MAY 2010, DOI: 10.1002/ajmg.b.31092

  9. DNA microsatellite and linkage analysis supports the inclusion of LOCR in the Rh blood group system


    Volume 43, Issue 4, April 2003, Pages: 440–444, Gail Coghlan and Teresa Zelinski

    Article first published online : 8 APR 2003, DOI: 10.1046/j.1537-2995.2003.00344.x

  10. Refined FISH characterization of a de novo 1p22–p36.2 paracentric inversion and associated 1p21–22 deletion in a patient with signs of 1p36 microdeletion syndrome

    American Journal of Medical Genetics

    Volume 99, Issue 4, 1 April 2001, Pages: 308–313, Palma Finelli, Daniela Giardino, Silvia Russo, Giulietta Gottardi, Francesca Cogliati, Graziano Grugni, Federka Natacci and Lidia Larizza

    Article first published online : 26 FEB 2001, DOI: 10.1002/ajmg.1181

  11. Fine deletion analysis of 1p36 chromosomal region in oral squamous cell carcinomas

    Journal of Oral Pathology & Medicine

    Volume 38, Issue 1, January 2009, Pages: 94–98, Mathieu Lefeuvre, Mehmet Gunduz, Hitoshi Nagatsuka, Esra Gunduz, Mahmoud Al Sheikh Ali, Levent Beder, Kunihiro Fukushima, Noboru Yamanaka, Kenji Shimizu and Noriyuki Nagai

    Article first published online : 23 MAR 2008, DOI: 10.1111/j.1600-0714.2008.00666.x

  12. Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma

    Clinical Endocrinology

    Volume 59, Issue 6, December 2003, Pages: 707–715, G. Opocher, F. Schiavi, A. Vettori, F. Pampinella, L. Vitiello, A. Calderan, B. Vianello, A. Murgia, M. Martella, A. Taccaliti, F. Mantero and M. L. Mostacciuolo

    Article first published online : 20 NOV 2003, DOI: 10.1046/j.1365-2265.2003.01910.x

  13. Identification of a minimal region of loss on the short arm of chromosome 1 in Wilms tumor

    Genes, Chromosomes and Cancer

    Volume 46, Issue 4, April 2007, Pages: 327–335, Yahya Tamimi, Kay Ziebart, Nancy Desaulniers, Kevin Dietrich and Paul Grundy

    Article first published online : 22 JAN 2007, DOI: 10.1002/gcc.20413

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    Haplotypes of the HRES-1 endogenous retrovirus are associated with development and disease manifestations of systemic lupus erythematosus

    Arthritis & Rheumatism

    Volume 58, Issue 2, February 2008, Pages: 532–540, Rudolf Pullmann Jr., Eduardo Bonilla, Paul E. Phillips, Frank A. Middleton and Andras Perl

    Article first published online : 31 JAN 2008, DOI: 10.1002/art.23161

  15. Discrete breakpoint mapping and shortest region of overlap of chromosome arm 1q gain and 1p loss in human hepatocellular carcinoma detected by semiquantitative microsatellite analysis

    Genes, Chromosomes and Cancer

    Volume 42, Issue 1, January 2005, Pages: 34–43, Takafumi Nishimura, Naoshi Nishida, Teruaki Itoh, Toshiki Komeda, Yoshihiro Fukuda, Iwao Ikai, Yoshio Yamaoka and Kazuwa Nakao

    Article first published online : 19 OCT 2004, DOI: 10.1002/gcc.20117

  16. Further evidence for a third deafness gene within the DFNA2 locus

    American Journal of Medical Genetics

    Volume 108, Issue 4, 1 April 2002, Pages: 304–309, Jayne A. Goldstein and Anil K. Lalwani

    Article first published online : 13 FEB 2002, DOI: 10.1002/ajmg.10299

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    Screening the genome for rheumatoid arthritis susceptibility genes: A replication study and combined analysis of 512 multicase families

    Arthritis & Rheumatism

    Volume 48, Issue 4, April 2003, Pages: 906–916, Damini Jawaheer, Michael F. Seldin, Christopher I. Amos, Wei V. Chen, Russell Shigeta, Carol Etzel, Aarti Damle, Xiangli Xiao, Dong Chen, Raymond F. Lum, Joanita Monteiro, Marlene Kern, Lindsey A. Criswell, Salvatore Albani, J. Lee Nelson, Daniel O. Clegg, Richard Pope, Harry W. Schroeder Jr., S. Louis Bridges Jr., David S. Pisetsky, Ryk Ward, Daniel L. Kastner, Ronald L. Wilder, Theodore Pincus, Leigh F. Callahan, Donald Flemming, Mark H. Wener and Peter K. Gregersen

    Article first published online : 3 APR 2003, DOI: 10.1002/art.10989

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    MUTYH c.933+3A>C, associated with a severely impaired gene expression, is the first Italian founder mutation in MUTYH-Associated Polyposis

    International Journal of Cancer

    Volume 132, Issue 5, 1 March 2013, Pages: 1060–1069, Elisa Pin, Chiara Pastrello, Rossella Tricarico, Laura Papi, Michele Quaia, Mara Fornasarig, Ileana Carnevali, Cristina Oliani, Alessio Fornasin, Marco Agostini, Roberta Maestro, Daniela Barana, Stefan Aretz, Maurizio Genuardi and Alessandra Viel

    Article first published online : 28 AUG 2012, DOI: 10.1002/ijc.27761

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    A tumor suppressor locus in familial and sporadic chordoma maps to 1p36

    International Journal of Cancer

    Volume 87, Issue 1, 1 July 2000, Pages: 68–72, Monica Miozzo, Leda Dalprà, Paola Riva, Marinella Volontà, Fabio Macciardi, Sergio Pericotti, M. Grazia Tibiletti, Michele Cerati, Klaus Rohde, Lidia Larizza and A. Maria Fuhrman Conti

    Article first published online : 2 JUN 2000, DOI: 10.1002/1097-0215(20000701)87:1<68::AID-IJC10>3.0.CO;2-V

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    Founder Effect and Estimation of the Age of the c.892C>T (p.Arg298Cys) Mutation in LMNA Associated to Charcot-Marie-Tooth Subtype CMT2B1 in Families from North Western Africa

    Annals of Human Genetics

    Volume 72, Issue 5, September 2008, Pages: 590–597, T. Hamadouche, Y. Poitelon, E. Genin, M. Chaouch, M. Tazir, N. Kassouri, S. Nouioua, A. Chaouch, I. Boccaccio, T. Benhassine, A. De Sandre-Giovannoli, D. Grid, N. Lévy and V. Delague

    Article first published online : 28 JUN 2008, DOI: 10.1111/j.1469-1809.2008.00456.x