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. Author manuscript; available in PMC: 2010 Jun 15.
Published in final edited form as: Dev Biol. 2009 Apr 8;330(2):305–317. doi: 10.1016/j.ydbio.2009.03.028

Table 2.

Embryos treated at HH 14 with either dose of cyclopamine were significantly different from control embryos (p=2.4×10−8) and each other (p=0.04), as determined with Fisher’s exact test.

Phenotype Control (n=13) 0.6 μg/μl CPA (n=16) 0.8 μg/μl CPA (n=14)
Hypoplastic pulmonary infundibulum* 0 3 1
Atretic pulmonary outlet* 0 6 3
Stenotic pulmonary ouetlet 0 2 0
Persistent truncus arteriosus 0 2 6
Unidentifiable single outlet 0 1 1
Normal 13 2 3
*

Both of these phenotypes were classified as pulmonary atresia based on the absence of a pulmonary artery.