Clinical Genetics

Cover image for Clinical Genetics

June 2000

Volume 57, Issue 6

Pages 409–463

  1. Mini Review

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Images in Genetics
    5. Original Article
    6. Short Reports
    7. Letters to the Editor
    8. Announcements
    1. Maternally inherited hearing impairment (pages 409–414)

      Guy Van Camp and Richard Jh Smith

      Version of Record online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570601.x

  2. HotSpots

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Images in Genetics
    5. Original Article
    6. Short Reports
    7. Letters to the Editor
    8. Announcements
    1. Expression profiling in cancer using gene chips (pages 415–416)

      Jamal Nasir

      Version of Record online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570602.x

    2. Interacting proteins in yeast – a perfect marriage (pages 416–417)

      Jamal Nasir

      Version of Record online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570602.1.x

    3. A genetic screen for suppression of polyglutamine induced toxicity in flies (pages 418–419)

      Jamal Nasir

      Version of Record online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570602.2.x

  3. Images in Genetics

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Images in Genetics
    5. Original Article
    6. Short Reports
    7. Letters to the Editor
    8. Announcements
  4. Original Article

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Images in Genetics
    5. Original Article
    6. Short Reports
    7. Letters to the Editor
    8. Announcements
    1. Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation (pages 423–429)

      Kye-Yoon Park, Marinos C Dalakas, Christina Semino-Mora, Hee-Suk Lee, Svetlana Litvak, Kazuyo Takeda, Victor J Ferrans and Lev G Goldfarb

      Version of Record online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570604.x

  5. Short Reports

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Images in Genetics
    5. Original Article
    6. Short Reports
    7. Letters to the Editor
    8. Announcements
    1. MEFV mutations in multiplex families with familial Mediterranean fever: is a particular genotype necessary for amyloidosis? (pages 430–434)

      Mustafa Tekin, Fatoş Yalçinkaya, Nilgün Çakar, Nejat Akar, Müge Mısırlıoğlu, Hakkı Taştan and Necmiye Tümer

      Version of Record online: 20 APR 2002 | DOI: 10.1034/j.1399-0004.2000.570605.x

    2. Hypogonadotrophic hypogonadism in Roifman syndrome (pages 435–438)

      Stephen P Robertson, Christine Rodda and Agnes Bankier

      Version of Record online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570606.x

    3. Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates (pages 439–443)

      Saïda Ben Arab, Mounira Hmani, Françoise Denoyelle, Amel Boulila-Elgaied, Sebastien Chardenoux, Slah Hachicha, Christine Petit and Hammadi Ayadi

      Version of Record online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570607.x

    4. Vertebral anomalies in a new family with ODED syndrome (pages 444–448)

      Linda D Piersall, S Bruce Dowton, William H McAlister and Darrel J Waggoner

      Version of Record online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570608.x

    5. Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri–Weill dyschondrosteosis (pages 449–453)

      G Palka, L Stuppia, P Guanciali Franchi, F Chiarelli, R Fischetto, P Borrelli, A Giannotti, G Fioretti, Mm Rinaldi, R Mingarelli, Ga Rappold and G Calabrese

      Version of Record online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570609.x

  6. Letters to the Editor

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Images in Genetics
    5. Original Article
    6. Short Reports
    7. Letters to the Editor
    8. Announcements
    1. Hemochromatosis in Galicia (NW Spain): a Celtic influence? (pages 454–455)

      Lola Soto, Ana Vega, Vicente Goyanes and Diana Valverde

      Version of Record online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570610.x

    2. The comparison of anthropometric variables in mentally retarded boys with and without fragile X syndrome (pages 456–458)

      Małgorzata Lisik, Krystyna Szymańska-Parkieta and Urszula Gałecka

      Version of Record online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570611.x

    3. Psychomotor development in Cri du Chat Syndrome (pages 459–461)

      Paola Cerruti Mainardi, Andrea Guala, Guido Pastore, Gloria Pozzo, Franca Dagna Bricarelli and Mauro Pierluigi

      Version of Record online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570612.x

  7. Announcements

    1. Top of page
    2. Mini Review
    3. HotSpots
    4. Images in Genetics
    5. Original Article
    6. Short Reports
    7. Letters to the Editor
    8. Announcements
    1. Workshop on Primed In Situ Labeling (PRINS) (page 462)

      Version of Record online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570613.x

    2. British Human Genetics Conference (page 463)

      Version of Record online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570614.x

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