Clinical Genetics

Cover image for Clinical Genetics

January 2000

Volume 57, Issue 1

Pages 1–92

  1. Mini Review

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Correspondence
  2. Hotspots

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Correspondence
    1. ‘New Age’ gene medicines for the 21st century (page 11)

      ME Suzanne Lewis

      Article first published online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570102.x

  3. Developmental Biology: Frontiers for Clinical Genetics

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Correspondence
    1. The molecular regulation of myogenesis (pages 16–25)

      Luc A Sabourin and Michael A Rudnicki

      Article first published online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570103.x

  4. Images in Genetics

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Correspondence
  5. Original Articles

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Correspondence
    1. Support for linkage of familial combined hyperlipidemia to chromosome 1q21–q23 in Chinese and German families (pages 29–34)

      Weidong Pei, Heike Baron, Bertram Müller-Myhsok, Hans Knoblauch, Said Ali Al-Yahyaee, Rutai Hui, Xigui Wu, Lisheng Liu, Andreas Busjahn, Friedrich C Luft and Herbert Schuster

      Article first published online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570105.x

    2. Assessment of education and counselling offered by a familial colorectal cancer clinic (pages 48–55)

      Veronica Collins, Jane Halliday, Rosemary Warren and Robert Williamson

      Article first published online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570107.x

    3. Partial CFTR genotyping and characterisation of cystic fibrosis patients with myocardial fibrosis and necrosis (pages 56–60)

      Jerzy Żebrak, Barbara Skuza, Andrzej Pogorzelski, Renata Ligarska, Ewa Kopytko, Jacek Pawlik, Ewa Rutkiewicz and Michal Witt

      Article first published online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570108.x

    4. An SRY-negative XX male with Huriez syndrome (pages 61–66)

      Patrizia Vernole, Alessandro Terrinoni, Biagio Didona, Vincenzo De Laurenzi, Pellegrino Rossi, Gerry Melino and Paola Grimaldi

      Article first published online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570109.x

  6. Short Reports

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Correspondence
    1. Identification of three novel mutations in the insulin receptor gene in type A insulin resistant patients (pages 67–69)

      Susanna Riqué, Carme Nogués, Lourdes Ibàñez, María Victoria Marcos, Juan Ferragut, Antonio Carrascosa and Neus Potau

      Article first published online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570110.x

    2. An unaffected individual from a breast/ovarian cancer family with germline mutations in both BRCA1 and BRCA2 (pages 70–73)

      Roxana Moslehi, Donna Russo, Catherine Phelan, Elaine Jack, Karen Antman and Steven Narod

      Article first published online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570111.x

    3. Correlations between individual clinical manifestations and CTG repeat amplification in myotonic dystrophy (pages 74–82)

      Corrado Marchini, Renata Lonigro , Lorenzo Verriello, Lucia Pellizzari, Paolo Bergonzi and Giuseppe Damante

      Article first published online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570112.x

  7. Letters to the Editor

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Correspondence
    1. The Haspeslagh syndrome (MIM 177980) is caused by an unbalanced reciprocal 6q/9p translocation (pages 83–85)

      Koenraad Devriendt, Maureen Holvoet, Alain De Mûelenaere and Jean-Pierre Fryns

      Article first published online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570113.x

    2. A further Angelman syndrome patient with UPD15 due to paternal meiosis II nondisjunction (pages 86–87)

      Cintia Fridman, Mara Santos, Íris Ferrari and Célia P Koiffmann

      Article first published online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570114.x

  8. Correspondence

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Developmental Biology: Frontiers for Clinical Genetics
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letters to the Editor
    9. Correspondence
    1. ‘Novel’ immunodeficiency syndrome may be a previously described entity (pages 90–91)

      Nancy J Carpenter, Izzet Berkel and Burhan Say

      Article first published online: 24 DEC 2001 | DOI: 10.1034/j.1399-0004.2000.570116.x

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