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There are 224216 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

    Version of Record online : 31 JAN 2002, DOI: 10.1002/ana.10106

  2. 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

    Version of Record online : 27 APR 2001, DOI: 10.1002/gcc.1139

  3. 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

    Version of Record online : 26 FEB 2001, DOI: 10.1002/ajmg.1181

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    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

    Version of Record online : 24 DEC 2001, DOI: 10.1046/j.1464-410x.2000.00837.x

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    Confirmation of genetic linkage between human systemic lupus erythematosus and chromosome 1q41

    Arthritis & Rheumatism

    Volume 42, Issue 9, September 1999, Pages: 1902–1907, Kathy L. Moser, Courtney Gray-McGuire, Jennifer Kelly, Neeraj Asundi, Hua Yu, Gail R. Bruner, Monique Mange, Robert Hogue, Barbara R. Neas and John B. Harley

    Version of Record online : 26 APR 2001, DOI: 10.1002/1529-0131(199909)42:9<1902::AID-ANR16>3.0.CO;2-G

  6. Clinical and genetic characterization of an autosomal dominant nephropathy

    American Journal of Medical Genetics

    Volume 99, Issue 3, 15 March 2001, Pages: 204–209, Ruti Parvari, Alla Shnaider, Anna Basok, Leonid Katchko, Zvi Borochovich, Adam Kanis and Daniel Landau

    Version of Record online : 6 FEB 2001, DOI: 10.1002/1096-8628(2001)9999:9999<::AID-AJMG1158>3.0.CO;2-P

  7. FISH characterization of a supernumerary r(1)(::cen[RIGHTWARDS ARROW]q22::q22[RIGHTWARDS ARROW]sq21::) chromosome associated with multiple anomalies and bilateral cataracts

    American Journal of Medical Genetics

    Volume 104, Issue 2, 22 November 2001, Pages: 157–164, Palma Finelli, Pietro Cavalli, Daniela Giardino, Giulietta Gottardi, Federica Natacci, Salvatore Savasta and Lidia Larizza

    Version of Record online : 2 OCT 2001, DOI: 10.1002/ajmg.10019

  8. Possible relationship between the van der Woude syndrome (vWS) locus and nonsyndromic cleft lip with or without cleft palate (NSCL/P)

    American Journal of Medical Genetics

    Volume 104, Issue 1, 15 November 2001, Pages: 86–92, Claude Houdayer, Catherine Bonaïti-Pellié, Caroline Erguy, Véronique Soupre, Marie-Gabrielle Dondon, Lydie Bürglen, Emmanuel Cougoureux, Rémy Couderc, Marie-Paule Vazquez and Michel Bahuau

    Version of Record online : 1 NOV 2001, DOI: 10.1002/1096-8628(20011115)104:1<86::AID-AJMG10053>3.0.CO;2-E

  9. 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

    Version of Record online : 13 FEB 2002, DOI: 10.1002/ajmg.10299

  10. 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

    Version of Record online : 23 MAR 2008, DOI: 10.1111/j.1600-0714.2008.00666.x

  11. Parkinson's genetics: An embarrassment of riches

    Annals of Neurology

    Volume 51, Issue 1, January 2002, Pages: 7–8, Katrina Gwinn-Hardy and Matt Farrer

    Version of Record online : 28 DEC 2001, DOI: 10.1002/ana.10091

  12. Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: Further delineation of partial trisomy 1q syndrome

    American Journal of Medical Genetics

    Volume 104, Issue 4, 15 December 2001, Pages: 312–318, Werner Emberger, E. Petek, P. M. Kroisel, H. Zierler and K. Wagner

    Version of Record online : 23 OCT 2001, DOI: 10.1002/ajmg.10096

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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

    Version of Record online : 1 FEB 1999, DOI: 10.1359/jbmr.1999.14.2.230

  14. 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

    Version of Record online : 14 DEC 2006, DOI: 10.1002/ajmg.b.30389

  15. Genetic studies of a family with hereditary hyperparathyroidism–jaw tumour syndrome

    Clinical Endocrinology

    Volume 50, Issue 2, February 1999, Pages: 191–196, Wassif S. Wassif, Filip Farnebo, Bin Tean Teh, Caje F. Moniz, Fang-Yuan Li, John D. Harrison, Timothy J. Peters, Catharina Larsson and Philip Harris

    Version of Record online : 24 DEC 2001, DOI: 10.1046/j.1365-2265.1999.00633.x

  16. Two cases of mosaic RhD blood-group phenotypes and paternal isodisomy for chromosome 1

    American Journal of Medical Genetics

    Volume 104, Issue 3, 1 December 2001, Pages: 250–256, Osamu Miyoshi, Ryuichi Yabe, Keiko Wakui, Yoshimitsu Fukushima, Shigeki Koizumi, Makoto Uchikawa, Tadashi Kajii, Chikahiko Numakura, Shunji Takahashi, Kiyoshi Hayasaka and Norio Niikawa

    Version of Record online : 25 OCT 2001, DOI: 10.1002/ajmg.10000

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    Studying the heterogeneity of brain tumors using medium throughput LOH analysis

    Cytometry

    Volume 47, Issue 1, 1 January 2002, Pages: 52–55, Oliver Bogler, Susan Finniss, Kanokwan Kittiniyom, Sandra Rempel, Mark Rosenblum, Tom Mikkelsen and Irene Newsham

    Version of Record online : 20 DEC 2001, DOI: 10.1002/cyto.10035

  18. Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31

    Annals of Neurology

    Volume 49, Issue 6, June 2001, Pages: 786–792, Stéphanie Baulac, Fabienne Picard, Alexandra Herman, Josué Feingold, Emmanuelle Genin, Edouard Hirsch, Jean-François Prud'Homme, Michel Baulac, Alexis Brice and Eric LeGuern

    Version of Record online : 2 APR 2001, DOI: 10.1002/ana.1014

  19. Linkage studies suggest a possible locus for developmental dyslexia on chromosome 1p

    American Journal of Medical Genetics

    Volume 105, Issue 1, 8 January 2001, Pages: 120–129, E.L. Grigorenko, F.B. Wood, M.S. Meyer, J.E.D. Pauls, L.A. Hart and D.L. Pauls

    Version of Record online : 2 JAN 2001, DOI: 10.1002/1096-8628(20010108)105:1<120::AID-AJMG1075>3.0.CO;2-T

  20. 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

    Version of Record online : 14 OCT 2002, DOI: 10.1002/ajmg.b.10757