1. Novel and recurrent COMP (cartilage oligomeric matrix protein) mutations in pseudoachondroplasia and multiple epiphyseal dysplasia

   • S. Ikegawa
   • Hirofumi Ohashi
   • Yusuke Nakamura

   Original investigation Pages: 633 - 638

2. Genomic structure and mutational spectrum of the bicistronic MOCS1 gene defective in molybdenum cofactor deficiency type A

   • J. Reiss
   • Ernst Christensen
   • Claude Dorche

   Original investigation Pages: 639 - 644

3. The structures of the human neuronal nicotinic acetylcholine receptor β2- and α3-subunit genes (CHRNB2 and CHRNA3)

   • Nicole Rempel
   • Sibilla Heyers
   • O. K. Steinlein

   Original investigation Pages: 645 - 653

4. FISH studies of the sperm of fathers of paternally derived cases of trisomy 21: no evidence for an increase in aneuploidy

   • M. Hixon
   • Elise Millie
   • Terry Hassold

   Original investigation Pages: 654 - 657

5. Refinement of genetic localization of the Alström syndrome on chromosome 2p12-13 by linkage analysis in a North African family

   • Françoise Macari
   • Corinne Lautier
   • F. Grigorescu

   Original investigation Pages: 658 - 661

6. Genomic structure of the human ezrin gene

   • P. Majander-Nordenswan
   • Markku Sainio
   • Antti Vaheri

   Original Investigation Pages: 662 - 665

7. CCG repeats in cDNAs from human brain

   • John J. Kleiderlein
   • Paul E. Nisson
   • R. L. Margolis

   Original investigation Pages: 666 - 673

8. A transcript map of an 800-kb region on human chromosome 11q13, part of the candidate region for SCA5 and BBS1

   • Shigui Zhu
   • D. S. Gerhard

   Original investigation Pages: 674 - 680

9. Characterization of mutations in patients with autoimmune polyglandular syndrome type 1 (APS1)

   • Cong-Yi Wang
   • Abdoreza Davoodi-Semiromi
   • J.-X. She

   Original investigation Pages: 681 - 685

10. A mutation (IVS8+0.6kbdelTC) creating a new donor splice site activates a cryptic exon in an Alu-element in intron 8 of the human β-glucuronidase gene

    • R. Vervoort
    • Richard Gitzelmann
    • Inge Liebaers

    Original investigation Pages: 686 - 693

11. Relaxation of imprinting in Prader-Willi syndrome

    • P. K. Rogan
    • James R. Seip
    • Joan H. M. Knoll

    Original investigation Pages: 694 - 701

12. Chromosomal fragile site expression in lymphocytes from patients with schizophrenia

    • Chia-Hsiang Chen
    • Hsuan-Hui Shih
    • K.-D. Wuu

    Original investigation Pages: 702 - 706

13. Identification of the 185delAG BRCA1 mutation in a Spanish Gypsy population

    • O. Díez
    • Montserrat Domènech
    • Montserrat Baiget

    Original investigation Pages: 707 - 708

14. Loss of heterozygosity in polycystic kidney disease with a missense mutation in the repeated region of PKD1

    • Michael Koptides
    • Rolandos Constantinides
    • C. Constantinou Deltas

    Original investigation Pages: 709 - 717

15. Complete mutational screening of the CFTR gene in 120 patients with pulmonary disease

    • C. Bombieri
    • Mariagiovanna Benetazzo
    • Pier Franco Pignatti

    Original investigation Pages: 718 - 722

16. Frequency of nucleated red blood cells in maternal blood during the different gestational ages

    • L. P. Shulman
    • Owen P. Phillips
    • S. S. Wachtel

    Original investigation Pages: 723 - 726

17. Detection of 6q deletions in breast carcinoma cell lines by fluorescence in situ hybridization

    • Yanming Zhang
    • Peter Matthiesen
    • B. Schlegelberger

    Short report Pages: 727 - 729

18. Mutations in the gene for the common gamma chain (γ_c) in X-linked severe combined immunodeficiency

    • Sebastian D. Fugmann
    • Susanna Müller
    • K. Schwarz

    Short report Pages: 730 - 731

19. Mutational spectrum of the iduronate-2-sulfatase (IDS) gene in 36 unrelated Russian MPS II patients

    • S. Karsten
    • Elena Voskoboeva
    • Marie-Louise Bondeson

    Short report Pages: 732 - 735