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Fig. 7. Thymus, thyroid and cardiovascular phenotype of Tbx1
conditional mutants shown by transverse histological sections. (A)
An E17.5 wild-type embryo with the thymus gland (tm) and the location of the
right subclavian artery (arrow) indicated. (B) A homozygous conditional
null embryo of the same stage shows thymus aplasia (asterisks), as well as the
presence of a retroesophageal right subclavian artery (RSA, arrow).
(C,D) The thyroid glands (th) of wild-type (C) and mutant (D) embryos
at E17.5. (E) Wild-type embryo shows normal separation of the aortic
(a) and pulmonary (p) trunks. (F) Abnormal septation of the outflow
tract results in persistent truncus arteriosus (PTA) in the mutant of the same
stage. (G-I) Sections through the heart show a ventricular septal
defect (VSD) in a Tbx1 homozygous conditional mutant (H) and a
Tbx1-/- embryo (I), compared with a wild-type litter mate
(G). (J-M) Transverse sections at E10.5 show normal development of
atria (A) and ventricles (V), as well as the outflow tract in both wild-type
(J,L) and conditional mutant (K,M) embryos. WT, wild type; PEKO/-, Tbx1
flox/null; Foxg1-Cre/+; -/-, Tbx1-/-. Scale bars: 300
µm in B,D,F; 100 µm in G-I; 50 µm in K,M.