Clinical Genetics

Cover image for Clinical Genetics

March 2006

Volume 69, Issue 3

Pages 199–296

  1. Perspectives

    1. Top of page
    2. Perspectives
    3. HotSpots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
  2. HotSpots

    1. Top of page
    2. Perspectives
    3. HotSpots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
  3. Original Articles

    1. Top of page
    2. Perspectives
    3. HotSpots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. A questionnaire study for 128 patients with Gaucher disease (pages 209–217)

      HJ Mankin, CA Trahan, NA Barnett, J Laughead, CM Bove and GM Pastores

      Article first published online: 12 JAN 2006 | DOI: 10.1111/j.1399-0004.2006.00573.x

    2. Comparative transcriptome maps: a new approach to the diagnosis of colorectal carcinoma patients using cDNA microarrays (pages 218–227)

      E Jansová, I Koutná, P Krontorád, Z Svoboda, S Křivánková, J Žaloudík, M Kozubek and S Kozubek

      Article first published online: 2 MAR 2006 | DOI: 10.1111/j.1399-0004.2006.00588.x

  4. Short Reports

    1. Top of page
    2. Perspectives
    3. HotSpots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. MLPA vs multiprobe FISH: comparison of two methods for the screening of subtelomeric rearrangements in 50 patients with idiopathic mental retardation (pages 228–233)

      M Palomares, A Delicado, P Lapunzina, D Arjona, C Amiñoso, J Arcas, A Martinez Bermejo, L Fernández and I López Pajares

      Article first published online: 8 FEB 2006 | DOI: 10.1111/j.1399-0004.2006.00567.x

    2. Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome (pages 234–238)

      V Shashi, MS Keshavan, TD Howard, MN Berry, MJ Basehore, E Lewandowski and TR Kwapil

      Article first published online: 12 JAN 2006 | DOI: 10.1111/j.1399-0004.2006.00569.x

    3. Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutations (pages 239–245)

      L-E Wehner, BJ Folz, L Argyriou, S Twelkemeyer, U Teske, UW Geisthoff, JA Werner, W Engel and K Nayernia

      Article first published online: 12 JAN 2006 | DOI: 10.1111/j.1399-0004.2006.00574.x

    4. A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability (pages 254–262)

      F Marroni, C Pastrello, P Benatti, M Torrini, D Barana, EL Cordisco, A Viel, C Mareni, C Oliani, M Genuardi, JE Bailey-Wilson, M Ponz de Leon and S Presciuttini

      Article first published online: 8 FEB 2006 | DOI: 10.1111/j.1399-0004.2006.00577.x

    5. Common variants of multiple genes that control reverse cholesterol transport together explain only a minor part of the variation of HDL cholesterol levels (pages 263–270)

      SM Boekholdt, OW Souverein, MWT Tanck, GK Hovingh, JA Kuivenhoven, RIG Peters, H Jansen, PMH Schiffers, EE Van Der Wall, PA Doevendans, PH Reitsma, AH Zwinderman, JJP Kastelein and JW Jukema

      Article first published online: 12 JAN 2006 | DOI: 10.1111/j.1399-0004.2006.00578.x

    6. A novel homozygous MMP2 mutation in a family with Winchester syndrome (pages 271–276)

      C Rouzier, R Vanatka, S Bannwarth, N Philip, A Coussement, V Paquis-Flucklinger and J-C Lambert

      Article first published online: 2 MAR 2006 | DOI: 10.1111/j.1399-0004.2006.00584.x

  5. Letters to the Editor

    1. Top of page
    2. Perspectives
    3. HotSpots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. HMLH1 and HMSH2 germline mutations in Greek families with hereditary non-polyposis colorectal cancer (pages 290–293)

      A Kataki, IP Gomatos, K Arapis, S Mparatsis, P Alepas, A Kaintatzis, M Nikolopoulou, E Leandros, MM Konstadoulakis and J Bramis

      Article first published online: 2 MAR 2006 | DOI: 10.1111/j.1399-0004.2006.00586.x

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