Cheryl L. Maslen
Department of Medicine
Oregon Health and Science University
Portland Oregon 97239
USA
Name/email consistency: high
- CRELD2: gene mapping, alternate splicing, and comparative genomic identification of the promoter region. Maslen, C.L., Babcock, D., Redig, J.K., Kapeli, K., Akkari, Y.M., Olson, S.B. Gene (2006)
- CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defects in Down syndrome. Maslen, C.L., Babcock, D., Robinson, S.W., Bean, L.J., Dooley, K.J., Willour, V.L., Sherman, S.L. Am. J. Med. Genet. A (2006)
- Molecular genetics of atrioventricular septal defects. Maslen, C.L. Curr. Opin. Cardiol. (2004)
- A rare branch-point mutation is associated with missplicing of fibrillin-2 in a large family with congenital contractural arachnodactyly. Maslen, C., Babcock, D., Raghunath, M., Steinmann, B. Am. J. Hum. Genet. (1997)