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. 2000 Jan;66(1):312-9.
doi: 10.1086/302723.

Involvement of the HLXB9 homeobox gene in Currarino syndrome

E Belloni, G Martucciello, D Verderio, E Ponti, M Seri, V Jasonni, M Torre, M Ferrari, L C Tsui, S W Scherer

Involvement of the HLXB9 homeobox gene in Currarino syndrome

E Belloni et al. Am J Hum Genet. 2000 Jan.
No abstract available

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Figures

Figure 1
Figure 1
a, ARM with total sacral agenesis and L5 hypoplasia in patient 020. b, Distal cologram, showing presence of a rectobulbar fistula. c and d, Hemisacrum as observed in CS (c) and in patient 015 (d). The MRI shows the presence of the anterior meningocele (AM).
Figure 2
Figure 2
Example of DG-DGGE (a) and direct DNA sequencing (b). a, Lanes A and B, Replicated samples frm patient 060. Lanes C and D, Controls. b, Electrophoregram showing two peaks (marked with an asterisk [*]) at the T248S mutation in patient 060.
See this image and copyright information in PMC

References

Electronic-Database Information

    1. Chromosome 7 Database, The, http://www.genet.sickkids.on.ca/chromosome7

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