Clinical Genetics

Cover image for Clinical Genetics

October 1993

Volume 44, Issue 4

Pages 169–224

  1. Original Article

    1. Top of page
    2. Original Article
    3. Letter to the Editor
    1. Prenatal diagnosis of fragile X syndrome by direct detection of the dynamic mutation due to an unstable DNA sequence (pages 169–172)

      Masatake Yamauchi, Shin Nagata, Naohiko Seki, Yoshiro Toyama, Naoki Harada, Norio Niikawa, Ichiro Masuno, Tadashi Kajii and Tada-aki Hori

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03873.x

    2. A family with autosomal dominant polycystic kidney disease not linked to chromosome 16p13.3 (pages 173–176)

      Steve Jeffery, Anand K. Saggar-Malik, Steve Morgan and Graham A. MacGregor

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03874.x

    3. Apolipoprotein B gene DNA polymorphisms are associated with macro- and microangiopathy in non-insulin-dependent diabetes mellitus (pages 177–184)

      Olavi Ukkola, Markku J. Savolainen, Pasi I. Salmela, Kai von Dickhoff and Y. Antero Kesäniemi

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03875.x

    4. Mosaic trisomy 16 in a thriving infant; maternal heterodisomy for chromosome 16 (pages 185–189)

      Noralane M. Lindor, Syeed M. Jalal, Stephen N. Thibodeau, Denise Bonde, Kristen L. Sauser and Pamela S. Karnes

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03876.x

    5. Oral-facial-digital syndrome with fibular aplasia: a new variant (pages 190–192)

      L. E. Figuera, F. Rivas and J. M. Cantú

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03877.x

    6. The Myhre syndrome: report of two cases (pages 203–207)

      D. Garcia-Cruz, L. E. Figuera, A. Feria-Velazco, J. Sánchez-Corona, M. O. Garcia-Cruz, R. M. Ramirez-Duenãs, A. Hernandez-Córdova, M. X. Ruiz, W. E. Bitar-Alatorre, M. L. Ramirez-Dueñas and J. M. Cantú

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03880.x

    7. Apple peel intestinal atresia in siblings with ocular anomalies and microcephaly (pages 208–210)

      Petter Strømme, Eilif Dahl, Tor Flage and Helge Stene-Johansen

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03881.x

    8. Dacryocystitis associated with osteopoikilosis (pages 211–213)

      I. Günal, S. Seber, N. Basaran, S. Artan, K. Günal and E. Gokturk

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03882.x

    9. Haplotype analysis at the low density lipoprotein receptor locus in normal and familial hypercholesterolemia Norwegian subjects (pages 214–220)

      Olaug K. Rødningen, Trond P. Leren, Oddveig Røsby, Serena Tonstad, Leiv Ose and Kare Berg

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03883.x

  2. Letter to the Editor

    1. Top of page
    2. Original Article
    3. Letter to the Editor
    1. Consanguineous marriages among parents of patients with Down syndrome (pages 221–222)

      A. I. Cereijo and M. L. Martínaz-frías

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03884.x

    2. Williams syndrome and subaortic stenosis (page 223)

      Nazmi Narin, Ruhi Özyürek, A. Rahmi Bakiler, Aytül Parlar, Müfit Arcasoy and Ferda Köprübaşsi

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03885.x

    3. Reply to the letter from Woods and Smith (page 224)

      R. H. Nyberg, A. K. Haapala and K. O. J. Simola

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03886.x

SEARCH

SEARCH BY CITATION