Clinical Genetics

Cover image for Clinical Genetics

November 1995

Volume 48, Issue 5

Pages 225–280

  1. Original Article

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Report on DNA Marker at Candidate Locus
    5. Letter to the Editor
    6. Announcements
    1. Chronological difference in walking impairment among Japanese group A xeroderma pigmentosum (XP-A) patients with various combinations of mutation sites (pages 225–231)

      Tomoko Maeda, Kenji Sato, Hironori Minami, Hiroyasu Taguchi and Kunihiko Yoshikawa

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04094.x

    2. Muscle expression of glucose-6-phosphate dehydrogenase deficiency in different variants (pages 232–237)

      Paolino Ninfali, Luciano Baronciani, Alessandra Bardoni and Nereo Bresolin

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04095.x

    3. Image quality in digital chromosome analysis systems (pages 238–242)

      S. Nivall, D. Holmquist, T. Gustavsson and J. Wahlström

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04096.x

    4. Apolipoprotein E allele frequencies in a South African Indian female population (pages 243–245)

      Nirmala Gounden, Jenisa Naidoo, Rosemary J. Pegoraro and G. Michael B. Berger

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04097.x

    5. Adenine phosphoribosyltransferase deficiency identified by urinary sediment analysis: cellular and molecular confirmation (pages 246–250)

      Chihiro Terai, Masayuki Hakoda, Hisashi Yamanaka, Naoyuki Kamatani, Mieko Okai, Fumiko Takahashi and Sadao Kashiwazaki

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04098.x

    6. Mitochondrial gene mutations in familial non-insulin-dependent diabetes mellitus in Taiwan (pages 251–254)

      Lee-Ming Chuang, Huey-Peir Wu, Ken C. Chiu, Chuen-Shiang Lai, Tong-Yuan Tai and Boniface J. Lin

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04099.x

    7. Pericentric inversions of chromosome 4: report of a new family and review of the literature (pages 255–260)

      A. Villa, M. Urioste, M. C. Carrascosa, S. Vázquez, A. Martínez and M. L. Martínez-Frías

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04100.x

    8. A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome (pages 261–263)

      Alberto E. Turco, Sandro Rossetti, M. Olivia Biasi, Gianfranco Rizzoni, Laura Massella, Niina H. Saarinen, Allessandra Renieri, Pier Franco Pignatti and Mario De Marchi

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04101.x

    9. A new syndrome with cardiac malformation, cleft lip-palate, microcephaly and digital anomalies? (pages 264–267)

      E. Ferda Perçin, Füsun Düzcan, Gülden Kafali and Ilhan Sezgin

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04102.x

    10. Christian's spondylo-digital syndrome: second familial case (pages 268–271)

      D. García-Cruz, J. M. Cantú, F. J. García-Martínez, M. O. García-Cruz, Z. Nazará, B. González-Ulloa, A. Hernández-Córdova, M. X. Ruíz and J. Sánchez-Corona

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04103.x

  2. Case Report

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Report on DNA Marker at Candidate Locus
    5. Letter to the Editor
    6. Announcements
    1. Pericentric inversion with a minute deletion of the Y chromosome in a severely oligozoospermic man (pages 272–274)

      Teruaki Iwamoto, Yutaka Nakahori, Yasuo Nakagome, Michitaka Yajima, Yoshiaki Satomi and Takao Osada

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04104.x

  3. Short Report on DNA Marker at Candidate Locus

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Report on DNA Marker at Candidate Locus
    5. Letter to the Editor
    6. Announcements
  4. Letter to the Editor

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Report on DNA Marker at Candidate Locus
    5. Letter to the Editor
    6. Announcements
    1. Down syndrome and systemic lupus erythematosus (page 277)

      Murray Feingold and Stuart Schneller

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04106.x

    2. Central nervous system abnormalities in chromosome deletion at 11q23: is it true? (pages 278–279)

      Orazio Gabrielli, Ugo Salvolini, Giovanni V. Coppa and Pierluigi Giorgi

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04107.x

  5. Announcements

    1. Top of page
    2. Original Article
    3. Case Report
    4. Short Report on DNA Marker at Candidate Locus
    5. Letter to the Editor
    6. Announcements
    1. Announcements (page 280)

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1995.tb04108.x

SEARCH

SEARCH BY CITATION