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{{Underlinked|date=June 2016}}
{{Infobox_gene}}
{{Infobox_gene}}
'''Split hand/foot malformation (ectrodactyly) type 3 pseudogene 1''', also known as '''SHFM3P1''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: SHFM3P1 split hand/foot malformation (ectrodactyly) type 3 pseudogene 1| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=26226| accessdate = }}</ref>
'''Split hand/foot malformation (ectrodactyly) type 3 pseudogene 1''', also known as '''SHFM3P1''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: SHFM3P1 split hand/foot malformation (ectrodactyly) type 3 pseudogene 1| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=26226| accessdate = }}</ref>
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID14702039.
Cenciarelli C, Chiaur DS, Guardavaccaro D, et al. (1999). "Identification of a family of human F-box proteins". Curr. Biol. 9 (20): 1177–9. doi:10.1016/S0960-9822(00)80020-2. PMID10531035.
Ianakiev P, Kilpatrick MW, Dealy C, et al. (1999). "A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24". Biochem. Biophys. Res. Commun. 261 (1): 64–70. doi:10.1006/bbrc.1999.0963. PMID10405324.
Chissoe SL, Bodenteich A, Wang YF, et al. (1995). "Sequence and analysis of the human ABL gene, the BCR gene, and regions involved in the Philadelphia chromosomal translocation". Genomics. 27 (1): 67–82. doi:10.1006/geno.1995.1008. PMID7665185.
Groffen J, Stephenson JR, Heisterkamp N, et al. (1984). "Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22". Cell. 36 (1): 93–9. doi:10.1016/0092-8674(84)90077-1. PMID6319012.
