Clinical Genetics

Cover image for Clinical Genetics

May 2002

Volume 61, Issue 5

Pages 321–392

  1. Mini Review

    1. Top of page
    2. Mini Review
    3. Hot Spots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. Inherited hypertrichoses (pages 321–329)

      D Garcia-Cruz, LE Figuera and JM Cantu

      Article first published online: 24 JUN 2002 | DOI: 10.1034/j.1399-0004.2002.610501.x

  2. Hot Spots

    1. Top of page
    2. Mini Review
    3. Hot Spots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. HotSpots (pages 330–334)

      J Nasir and B Liu

      Article first published online: 24 JUN 2002 | DOI: 10.1034/j.1399-0004.2002.610502.x

  3. Original Articles

    1. Top of page
    2. Mini Review
    3. Hot Spots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. Attention-deficit/hyperactivity disorder (ADHD): feasibility of linkage analysis in a genetic isolate using extended and multigenerational pedigrees (pages 335–343)

      M Arcos-Burgos, FX Castellanos, F Lopera, D Pineda, JD Palacio, M Garcia, GC Henao, LG Palacio, K Berg, JE Bailey-Wilson and M Muenke

      Article first published online: 24 JUN 2002 | DOI: 10.1034/j.1399-0004.2002.610503.x

    2. Inducible nitric oxide synthase gene and diabetic retinopathy in Asian Indian patients (pages 344–348)

      G Kumaramanickavel, S Sripriya, RN Vellanki, NK Upadyay, SS Badrinath, V Rajendran, B Sukumar, VL Ramprasad and T Sharma

      Article first published online: 24 JUN 2002 | DOI: 10.1046/j.0009-9163.2002.00251.x

  4. Short Reports

    1. Top of page
    2. Mini Review
    3. Hot Spots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. New mutations in the CBFA1 gene in two Mexican patients with cleidocranial dysplasia (pages 349–353)

      L Machuca-Tzili, N Monroy-Jaramillo, A González-del Angel and S Kofman-Alfaro

      Article first published online: 24 JUN 2002 | DOI: 10.1034/j.1399-0004.2002.610505.x

    2. De novo MECP2 frameshift mutation in a boy with moderate mental retardation, obesity and gynaecomastia (pages 359–362)

      T Kleefstra, HG Yntema, AR Oudakker, T Romein, E Sistermans, W Nillessen, H Van Bokhoven, BBA De Vries and BCJ Hamel

      Article first published online: 24 JUN 2002 | DOI: 10.1034/j.1399-0004.2002.610507.x

    3. A patient homozygous for the SCA6 gene with retinitis pigmentosa (pages 375–379)

      T Fukutake, I Kamitsukasa, K Arai, T Hattori and T Nakajima

      Article first published online: 24 JUN 2002 | DOI: 10.1034/j.1399-0004.2002.610510.x

    4. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome (pages 380–383)

      P Sandrin-Garcia, C Macedo, LR Martelli, ES Ramos, ML Guion-Almeida, A Richieri-Costa and GAS Passos

      Article first published online: 24 JUN 2002 | DOI: 10.1034/j.1399-0004.2002.610511.x

  5. Letters to the Editor

    1. Top of page
    2. Mini Review
    3. Hot Spots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. MECP2 mutations in Swedish Rett syndrome clusters (pages 384–385)

      F Xiang, Y Stenbom and M Anvret

      Article first published online: 24 JUN 2002 | DOI: 10.1034/j.1399-0004.2002.610512.x

    2. Familial pericentric inversion of chromosome 4: inv(4)(p16.1q12) (pages 386–388)

      F Stipoljev, M Stanojevic and A Kurjak

      Article first published online: 24 JUN 2002 | DOI: 10.1034/j.1399-0004.2002.610513.x

    3. High prevalence of I179S mutation in patients with late-onset metachromatic leukodystrophy (pages 389–390)

      A Lugowska, J Berger, A Tylki-Szymañska, B Czartoryska, B Löschl and B Molzer

      Article first published online: 24 JUN 2002 | DOI: 10.1034/j.1399-0004.2002.610514.x

    4. Early development of megarectum in myotonic dystrophy (pages 391–392)

      B Meijers, M Miserez, G Veereman-Wouters and JP Fryns

      Article first published online: 24 JUN 2002 | DOI: 10.1034/j.1399-0004.2002.610515.x

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