Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome

F K Wong, H Koillinen, J Rautio, B T Teh, R Ranta, A Karsten, O Larson, S Linder-Aronson, J Huggare, Catharina Larsson, Juha Kere

    Research output: Contribution to journalArticleScientificpeer-review

    Original languageEnglish
    JournalJournal of Medical Genetics
    Volume2001
    Issue number38
    Pages (from-to)198-202
    Number of pages5
    ISSN0022-2593
    Publication statusPublished - 2001
    MoE publication typeA1 Journal article-refereed

    Fields of Science

    • VANDERWOUDE SYNDROME
    • LINKAGE ANALYSIS
    • CRITICAL REGION
    • 1Q32-Q41
    • MAP
    • 311 Basic medicine

    Cite this

    Wong, F. K., Koillinen, H., Rautio, J., Teh, B. T., Ranta, R., Karsten, A., Larson, O., Linder-Aronson, S., Huggare, J., Larsson, C., & Kere, J. (2001). Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome. Journal of Medical Genetics, 2001(38), 198-202.