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Marfan syndrome is closely linked to a marker on chromosome 15q1.5----q2.1.
Author(s) -
Petros Tsipouras,
M. Sarfarazi,
Anne S. Devi,
Barbara Weiffenbach,
M. Boxer
Publication year - 1991
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.88.10.4486
Subject(s) - marfan syndrome , locus (genetics) , genetics , genetic linkage , connective tissue disorder , etiology , biology , chromosome , genetic marker , gene , medicine , pathology
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.

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