Spectrum of mutations and genotype–phenotype analysis in Currarino syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/5200683.pdf
Reference22 articles.
1. Currarino G, Coln D, Votteler T . Triad of anorectal, sacral, and presacral anomalies AJR Am J Roentgenol 1981 137: 395–398
2. Lynch SA, Bond PM, Copp AJ et al. A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36 Nat Genet 1995 11: 93–95
3. Ross AJ, Ruiz Perez V, Wang Y et al. A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis Nat Genet 1998 20: 358–361
4. Levine M, Rubin GM, Tjian R . Human DNA sequences homologous to a protein coding region conserved between homeotic genes of Drosophila Cell 1984 38: 667–673
5. Gerard M, Zakany J, Duboule D . Interspecies exchange of a Hoxd enhancer in vivo induces premature transcription and anterior shift of the sacrum Dev Biol 1997 190: 32–40
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