AUB ScholarWorks

Browsing by Subject "FABP2 gene"

Browsing by Subject "FABP2 gene"

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  • Kurban M.; Kim C.A.; Kiuru M.; Fantauzzo K.; Cabral R.; Abbas O.; Levy B.; Christiano A.M. (BASELALLSCHWILERSTRASSE 10, CH-4009 BASEL, SWITZERLAND, 2011)
    Background: Cantu syndrome is a rare condition which is characterized clinically by hypertrichosis, cardiomegaly and bone abnormalities. Inherited hypertrichoses are very rare human disorders whose incidence has been ...

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