Clinical Genetics

Cover image for Clinical Genetics

September 1991

Volume 40, Issue 3

Pages 177–256

  1. Announcing a New Category of Papers

    1. Top of page
    2. Announcing a New Category of Papers
    3. Original Article
    4. Case Report
    5. Rapid Short Communication
    6. Letters to the Editors
    7. DNA Report
    1. DNA markers in candidate genes (page 177)

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03072.x

  2. Original Article

    1. Top of page
    2. Announcing a New Category of Papers
    3. Original Article
    4. Case Report
    5. Rapid Short Communication
    6. Letters to the Editors
    7. DNA Report
    1. Association of a genetic polymorphism in human apolipoprotein B-100 with intermediate density lipoprotein concentrations (pages 178–185)

      Miguel T. Robinson, René Butler and Ronald M. Krauss

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03073.x

    2. Trembling chin — a report of this inheritable dominant character in a four-generation Canadian family (pages 186–189)

      Dale E. Alsager, Peter Bowen and J. S. Bamforth

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03074.x

    3. Enhancement of amniotic fluid cell growth for genetic amniocentesis (pages 190–193)

      Thomas Mathews and Ram S. Verma

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03075.x

    4. Absence of predictable phenotypic expression in proximal 15q duplications (pages 194–201)

      Carol J. Ludowese, Kate J. Thompson, Gurbax S. Sekhon and Richard M. Pauli

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03076.x

    5. EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) with a balanced reciprocal translocation between 7q11.21 and 9p12 (or 7p11.2 and 9q12) in three generations (pages 202–206)

      Tomonobu Hasegawa, Yukihiro Hasegawa, Shinji Asamura, Toshiro Nagai, Yutaka Tsuchiya, Makoto Ninomiya and Yoshimitsu Fukushima

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03077.x

    6. Patients with deletions of 9q22q34 do not define a syndrome: three case reports and a literature review (pages 207–214)

      S. A. Farrell, J. Siegel-Bartelt and I. Teshima

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03078.x

    7. Nine mutations in the cystic fibrosis (CF) gene account for 80% of the CF chromosomes in French patients (pages 218–224)

      B. Simon-Bouy, E. Mornet, J. L. Serre, A. Taillandier, J. Boué and A. Boué

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03080.x

    8. Poland-Moebius syndrome in a boy and Poland syndrome in his mother (pages 225–228)

      A. Rojas-Martínez, D. García-Cruz, A. Rodríguez García, J. Sánchez-Corona and F. Rivas

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03081.x

  3. Case Report

    1. Top of page
    2. Announcing a New Category of Papers
    3. Original Article
    4. Case Report
    5. Rapid Short Communication
    6. Letters to the Editors
    7. DNA Report
    1. Smith-Lemli-Opitz syndrome in female, monozygotic twins (pages 229–232)

      G. Tzouvelekis, K. Antoniades, A. Batma and Ch. Nanas

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03082.x

    2. Identification of a marker chromosome as inv dup(15) by molecular analysis (pages 233–236)

      Yoshitaka Shibuya, Hidefumi Tonoki, Naofumi Kajii and Norio Niikawa

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03083.x

    3. Cell line segregation in a 45,X/46,XY mosaic child with asymmetric leg growth (pages 237–241)

      Peter R. Papenhausen, O. Thomas Mueller, Barry Bercu, Jose Salazar and Thomas A. Tedesco

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03084.x

  4. Rapid Short Communication

    1. Top of page
    2. Announcing a New Category of Papers
    3. Original Article
    4. Case Report
    5. Rapid Short Communication
    6. Letters to the Editors
    7. DNA Report
    1. Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP-met30) (pages 242–246)

      Gösta Holmgren, Lars Steen, Jan Ekstedt, Carl-Gustav Groth, B.-G. Ericzon, Siv Eriksson, Oluf Andersen, Ingvar Karlberg, Gunnela Nordén, Masamitsu Nakazato, Philip Hawkins, Suzanne Richardson and Mark Pepys

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03085.x

  5. Letters to the Editors

    1. Top of page
    2. Announcing a New Category of Papers
    3. Original Article
    4. Case Report
    5. Rapid Short Communication
    6. Letters to the Editors
    7. DNA Report
    1. Balanced pericentric inversion 8(p23q13) in a child with rhizomelic chondrodysplasia punctata and his mother (pages 247–248)

      Silvia Castillo-Taucher, Juan Pable Beca, Raúl Sáez and Verónica Geldres

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03086.x

    2. Hypoplasia of the corpus callosum and growth hormone deficiency in a boy with the XXXXY syndrome (pages 249–250)

      G. Haeusler, H. Frisch, Z. Guchev, F. Hadziselimovic, A. Neuhold and W. Vormittag

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03087.x

    3. Insulin-dependent diabetes developed in a young man with Bloom's syndrome (pages 251–252)

      Naomi Kondo, Junichi Asano, Shoko Kimura, Tomomi Asano and Tadao Orii

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03088.x

    4. Acrodysgenital dwarfism or Smith-Lemli-Opitz type II syndrome (page 252)

      Martine Le Merrer

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03089.x

    5. First treatment of family with hereditary adductor cord paralysis (pages 253–254)

      J. D. T. Mason, G. E. Murty and P. J. Bradley

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03090.x

    6. Mosaic trisomy 8 associated with jejunal duplication (pages 254–255)

      R. Curtis Rogers, T. David Marsh, Prithvi Reddy and Donna Lett

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03091.x

  6. DNA Report

    1. Top of page
    2. Announcing a New Category of Papers
    3. Original Article
    4. Case Report
    5. Rapid Short Communication
    6. Letters to the Editors
    7. DNA Report
    1. A Taql RFLP at the human renal kallikrein (KLK1) locus (page 256)

      K. E. Berge and K. Berg

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1991.tb03092.x

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