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    Proc Natl Acad Sci U S A. 1991 May 15;88(10):4486-8.

    Marfan syndrome is closely linked to a marker on chromosome 15q1.5----q2.1.

    Source

    Department of Pediatrics, University of Connecticut Health Center, Farmington 06030.

    Abstract

    Marfan syndrome is a systemic disorder of the connective tissue inherited as an autosomal dominant trait. The disorder imparts significant morbidity and mortality. The etiology of the disorder remains elusive. A recent study localized the gene for Marfan syndrome on chromosome 15. We present data showing that marker D15S48 is genetically linked to Marfan syndrome. Pairwise linkage analysis gave a maximum lod (logarithm of odds) score of Z = 11.78 at theta = 0.02. Furthermore our data suggest that the Marfan syndrome locus is possibly flanked on either side by D15S48 and D15S49.

    PMID:
    2034688
    [PubMed - indexed for MEDLINE]
    PMCID:
    PMC51685
    Free PMC Article

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