Clinical Genetics

Cover image for Clinical Genetics

January 1997

Volume 51, Issue 1

Pages 1–79

  1. Original Article

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Communication
    5. Original Article
    1. “Reduction” of CGG trinucleotide expansion from mother to offspring in seven fragile-X families (pages 1–6)

      Danuta Z. Loesch, Vida Petrovic, David I. Francis, Ralph Oertel and Howard Slater

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02405.x

    2. Symmetry of neurological signs in Pakistani patients with probable inherited spastic cerebral palsy (pages 7–14)

      Simon Mitchell and Sarah Bundey

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02406.x

    3. The role of the apolipoprotein E polymorphism in the prediction of coronary artery disease age of onset (pages 22–25)

      Jason H. Moore, Sharon L Reilly, Robert E. Ferrell and Charles F. Sing

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02408.x

    4. Association analysis of CA repeat polymorphism of the endothelial nitric oxide synthase gene with essential hypertension in Japanese (pages 26–30)

      T. Nakayama, M. Soma, Y. Takahashi, Y. Izumi, K. Kanmatsuse and M. Esumi

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02409.x

    5. Association of angiotensin II type 1 receptor gene polymorphism with essential hypertension (pages 31–34)

      William Y. S. Wang, Robert L Zee and Brian J. Morris

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02410.x

    6. Genetic variation of the angiotensin-converting enzyme gene: increased frequency of the insertion allele in Koreans (pages 35–38)

      S. H. Hong, B. Y. Kang, W. H. Park, J. Q. Kim and C. C. Lee

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02411.x

    7. Are common mutations of cystathionine β-synthase involved in the aetiology of neural tube defects? (pages 39–42)

      D. Ramsbottom, J.M. Scott, A. Molloy, D. G. Weir, P. N. Kirke, J. L. Mills, P. M. Gallagher and A. S. Whitehead

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02412.x

    8. Spectrum of CFTR mutations in Argentine cystic fibrosis patients (pages 43–47)

      Lilien Chertkoff, Alejandra Visich, Thierry Bienvenu, Mario Grenoville, Edgardo Segal, Luis Carniglia, Jean Claude Kaplan and Cristina Barreiro

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02413.x

    9. Interstitial deletion of long arm of chromosome no. 5 with growth hormone deficiency-an emerging syndrome? (pages 48–51)

      Jyoti Krishna, Terry L Myers, Michael J. Bourgeois and Vijay Tonk

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02414.x

    10. Oculopharyngeal muscular dystrophy (OPMD)-report and genetic studies of an Australian kindred (pages 52–55)

      Bin Tean Teh, Alice-Ann Sullivan, Filip Farnebo, Cecilia Zander, Fang Yuan Li, Noela Strachan, Martin Schalling, Catharina Larsson and Paul Sandstrom

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02415.x

  2. Case Report

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Communication
    5. Original Article
    1. De novo duplication of 7pter[RIGHTWARDS ARROW]p21.2 and deletion of 9pter[RIGHTWARDS ARROW]p23.5: clinical and cytogenetic diagnosis (pages 56–60)

      E. Back, C. Jung, S. Zeitler and W. Schempp

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02416.x

    2. An autosomal recessive adducted thumb-club foot syndrome observed in Turkish cousins (pages 61–64)

      Munis Dundar, Fatma Demiryilmaz, Ilhan Demiryilmaz, Sefer Kumandas, Kuddusi Erkilic, Mustafa Kendirci, Mehmet Tuncel, Isilay Ozyazgan and John L Tolmie

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02417.x

    3. Two mosaic-YY males carrying asymmetric Y chromosomes (pages 65–68)

      L. Zelante, B. Dallapiccola, S. Calvano, E. Memeo, P. Gasparini, P. Simi, S. Rossi, P. Finelli, M. Rocchi and N. Archidiacono

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02418.x

    4. Paracentric inversion of chromosome 9 with schizoaffective disorder (pages 69–70)

      Yasuhiro Inayama, Hiroshi Yoneda, Kentaro Fukushima, Jun Sakai, Hiroyuki Asaba and Toshiaki Sakai

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02419.x

  3. Short Communication

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Communication
    5. Original Article
    1. Chromosome deletion 17pl 1.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation (pages 71–74)

      F. Behjati, M. Mullarkey, A. Bergbaum, A. C. Berry and Z. Docherty

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02420.x

  4. Original Article

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Communication
    5. Original Article
    1. Short Report on DNA Marker at Candidate Locus : A new restriction-site polymorphism in the human proteolipid protein gene (page 75)

      Chiaki Kawanishi, Hitoshi Osaka, Ken Inoue, Hideki Onishi, Yoshiteru Yamada and Kenji Kosaka

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02421.x

    2. Short Report on DNA Marker at Candidate Locus : A fok 1 polymorphism in the human neuronal nicotinic acetylcholine receptor α4 subunit gene (pages 78–79)

      Michel Guipponi, Michel Baldy-Moulinier and Alain Malafosse

      Article first published online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1997.tb02423.x

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