Human Mutation

Cover image for Human Mutation

1995

Volume 6, Issue 4

Pages fmi–fmi, 281–354

  1. Masthead

    1. Top of page
    2. Masthead
    3. Review Articles
    4. Mutation Updates
    5. Rapid Communications
    6. Research Articles
    7. Methods
    8. Mutation in Briefs
    1. Masthead (page fmi)

      Version of Record online: 1 JUN 2005 | DOI: 10.1002/humu.1380060401

  2. Review Articles

    1. Top of page
    2. Masthead
    3. Review Articles
    4. Mutation Updates
    5. Rapid Communications
    6. Research Articles
    7. Methods
    8. Mutation in Briefs
  3. Mutation Updates

    1. Top of page
    2. Masthead
    3. Review Articles
    4. Mutation Updates
    5. Rapid Communications
    6. Research Articles
    7. Methods
    8. Mutation in Briefs
    1. Molecular genetics of muccpolysaccharidosis type I: Diagnostic, clinical, and biological implications (pages 288–302)

      Hamish S. Scott, Susanna Bunge, Andreas Gal, Lome A. Clarke, C. Phillip Morris and John J. Hopwood

      Version of Record online: 1 JUN 2005 | DOI: 10.1002/humu.1380060403

  4. Rapid Communications

    1. Top of page
    2. Masthead
    3. Review Articles
    4. Mutation Updates
    5. Rapid Communications
    6. Research Articles
    7. Methods
    8. Mutation in Briefs
    1. Analysis of mutational changes at the HLA locus in single human sperm (pages 303–310)

      Mei-Mei Huang, Henry A. Erlich, Myron F. Goodman and Norman Arnheim

      Version of Record online: 1 JUN 2005 | DOI: 10.1002/humu.1380060404

  5. Research Articles

    1. Top of page
    2. Masthead
    3. Review Articles
    4. Mutation Updates
    5. Rapid Communications
    6. Research Articles
    7. Methods
    8. Mutation in Briefs
    1. Cystic fibrosis mutation analysis: Report from 22 U.K. regional genetics laboratories (pages 326–333)

      Martin J. Schwarz, Geraldine M. Malone, Andrea Haworth, Jeremy P. Cheadle, A. Linda Meredith, Anne Gardner, I. Hilary Sawyer, Margaret Connarty, Nick Dennis, Anneke Seller, Ann Harris, Rohan Taylor, Simon Dear, Helen Middleton-Price, Cathie McMahon, Ed Mayall, Rob McMahon, David E. Barton, Martin Giles, Victoria Lindley, Davinder S. Plaha, Susan Price, Abid Sharif, Gareth S. Cross, Ann Dalton, Graham Taylor, Andrew Wallace, Mayada Tassabehji, Joanne L. Whittaker, Rachel Butler, Ann Curtis, Ros Pinkett, Annette J. Gilfillan, David J. H. Brock, G. Scott Higgins, George Lanyon, Zosia Miedzybrodzka, Mark Davidson, Colin A. Graham and Alison J. M. Hill

      Version of Record online: 1 JUN 2005 | DOI: 10.1002/humu.1380060406

    2. French CF family genotype analysis shows that the R297Q mutation is a rare polymorphism (pages 334–335)

      Ian Dorval, Pascal Jézéquel, Bruno Chauvel, Christèle Dubourg, Patricia Fergelot, Jean Yves Le Gall, Michel Roussey and Martine Blayau

      Version of Record online: 1 JUN 2005 | DOI: 10.1002/humu.1380060407

  6. Methods

    1. Top of page
    2. Masthead
    3. Review Articles
    4. Mutation Updates
    5. Rapid Communications
    6. Research Articles
    7. Methods
    8. Mutation in Briefs
    1. Efficient strategy for the detection of mutations in acrogeric Ehlers-danlos syndrome type IV (pages 336–342)

      P. H. Johnson, A. J. Richards, J. C. Lloyd, F. M. Pope and D. A. Hopkinson

      Version of Record online: 1 JUN 2005 | DOI: 10.1002/humu.1380060408

  7. Mutation in Briefs

    1. Top of page
    2. Masthead
    3. Review Articles
    4. Mutation Updates
    5. Rapid Communications
    6. Research Articles
    7. Methods
    8. Mutation in Briefs
    1. A 12-bp deletion ( 7818del12 ) in the c-kit protooncogene in a large Italian kindred with piebaldism (pages 343–345)

      Paola Riva, Nicoletta Milani, Paola Gandolfi and Lidia Larizza

      Version of Record online: 1 JUN 2005 | DOI: 10.1002/humu.1380060409

    2. Twenty-five novel mutations of the factor IX gene in haemophilia B (pages 346–348)

      Karin Wulff, Winnie Schröder, Manfred Wehnert and Falko H. Herrmann

      Version of Record online: 1 JUN 2005 | DOI: 10.1002/humu.1380060410

    3. Mutations of butyrylcholinesterase gene in a family with hypocholinesterasemia (pages 349–351)

      Sayomi Iida, Masahiro Kinoshita, Hiroshi Fujii, Yasuhiro Moriyama, Yasushi Nakamura, Noboru Yura and Kaname Moriwaki

      Version of Record online: 1 JUN 2005 | DOI: 10.1002/humu.1380060411

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