ALX4

Aristaless-like homeobox 4, also known as ALX4, is a human gene.cite web | title = Entrez Gene: ALX4 aristaless-like homeobox 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=60529| accessdate = ]

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References

Further reading

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*cite journal | author=Bartsch O, Wuyts W, Van Hul W, "et al." |title=Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11. |journal=Am. J. Hum. Genet. |volume=58 |issue= 4 |pages= 734–42 |year= 1996 |pmid= 8644736 |doi=
*cite journal | author=Qu S, Tucker SC, Zhao Q, "et al." |title=Physical and genetic interactions between Alx4 and Cart1. |journal=Development |volume=126 |issue= 2 |pages= 359–69 |year= 1999 |pmid= 9847249 |doi=
*cite journal | author=Wu YQ, Badano JL, McCaskill C, "et al." |title=Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome. |journal=Am. J. Hum. Genet. |volume=67 |issue= 5 |pages= 1327–32 |year= 2000 |pmid= 11017806 |doi=
*cite journal | author=Wuyts W, Cleiren E, Homfray T, "et al." |title=The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500). |journal=J. Med. Genet. |volume=37 |issue= 12 |pages= 916–20 |year= 2001 |pmid= 11106354 |doi=
*cite journal | author=Mavrogiannis LA, Antonopoulou I, Baxová A, "et al." |title=Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects. |journal=Nat. Genet. |volume=27 |issue= 1 |pages= 17–8 |year= 2001 |pmid= 11137991 |doi= 10.1038/83703
*cite journal | author=Nagase T, Nakayama M, Nakajima D, "et al." |title=Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. |journal=DNA Res. |volume=8 |issue= 2 |pages= 85–95 |year= 2001 |pmid= 11347906 |doi=
*cite journal | author=Boras K, Hamel PA |title=Alx4 binding to LEF-1 regulates N-CAM promoter activity. |journal=J. Biol. Chem. |volume=277 |issue= 2 |pages= 1120–7 |year= 2002 |pmid= 11696550 |doi= 10.1074/jbc.M109912200
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Wakui K, Gregato G, Ballif BC, "et al." |title=Construction of a natural panel of 11p11.2 deletions and further delineation of the critical region involved in Potocki-Shaffer syndrome. |journal=Eur. J. Hum. Genet. |volume=13 |issue= 5 |pages= 528–40 |year= 2005 |pmid= 15852040 |doi= 10.1038/sj.ejhg.5201366
*cite journal | author=Mavrogiannis LA, Taylor IB, Davies SJ, "et al." |title=Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype. |journal=Eur. J. Hum. Genet. |volume=14 |issue= 2 |pages= 151–8 |year= 2006 |pmid= 16319823 |doi= 10.1038/sj.ejhg.5201526

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