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Journal of Dental Research, Vol. 81, No. 7,
492-496 (2002)
DOI: 10.1177/154405910208100712
Cystic Fibrosis Transmembrane Regulator Gene (CFTR) is Associated with Abnormal Enamel Formation
C.K. Arquitt1,
C. Boyd2 and
J.T. Wright2,*
1 Private Practice, Pediatric Dentistry, Nashville, TN; and
2 Department of Pediatric Dentistry, School of Dentistry, Brauer Hall CB #7450, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7450;

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Figure. Amplification of CFTR RNA was seen in the wild-type mouse intestine (Co-I) and tooth bud (Co-T) but was not observed in the matched CF mouse tissues (CF-I = intestine; CF-T = tooth bud).
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