Daftary GS، Taylor HS (2001). "Implantation in the human: the role of HOX genes". Seminars in Reproductive Medicine. ج. 18 ع. 3: 311–20. DOI:10.1055/s-2000-12568. PMID:11299969.
Daftary GS، Taylor HS (يونيو 2001). "Molecular markers of implantation: clinical implications". Current Opinion in Obstetrics and Gynecology. ج. 13 ع. 3: 269–74. DOI:10.1097/00001703-200106000-00004. PMID:11396649.
Davies JA، Fisher CE (2002). "Genes and proteins in renal development". Experimental Nephrology. ج. 10 ع. 2: 102–13. DOI:10.1159/000049905. PMID:11937757.
Eun Kwon H، Taylor HS (ديسمبر 2004). "The role of HOX genes in human implantation". Annals of the New York Academy of Sciences. ج. 1034: 1–18. DOI:10.1196/annals.1335.001. PMID:15731295.
Apiou F، Flagiello D، Cillo C، Malfoy B، Poupon MF، Dutrillaux B (1996). "Fine mapping of human HOX gene clusters". Cytogenetics and Cell Genetics. ج. 73 ع. 1–2: 114–5. DOI:10.1159/000134320. PMID:8646877.
Potter SS، Branford WW (أكتوبر 1998). "Evolutionary conservation and tissue-specific processing of Hoxa 11 antisense transcripts". Mammalian Genome. ج. 9 ع. 10: 799–806. DOI:10.1007/s003359900870. PMID:9745033.
Taylor HS، Igarashi P، Olive DL، Arici A (مارس 1999). "Sex steroids mediate HOXA11 expression in the human peri-implantation endometrium". The Journal of Clinical Endocrinology and Metabolism. ج. 84 ع. 3: 1129–35. DOI:10.1210/jc.84.3.1129. PMID:10084606.
Thompson AA، Nguyen LT (ديسمبر 2000). "Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation". Nature Genetics. ج. 26 ع. 4: 397–8. DOI:10.1038/82511. PMID:11101832.
Fujino T، Suzuki A، Ito Y، Ohyashiki K، Hatano Y، Miura I، Nakamura T (فبراير 2002). "Single-translocation and double-chimeric transcripts: detection of NUP98-HOXA9 in myeloid leukemias with HOXA11 or HOXA13 breaks of the chromosomal translocation t(7;11)(p15;p15)". Blood. ج. 99 ع. 4: 1428–33. DOI:10.1182/blood.V99.4.1428. PMID:11830496.
Kosaki K، Kosaki R، Suzuki T، Yoshihashi H، Takahashi T، Sasaki K، Tomita M، McGinnis W، Matsuo N (فبراير 2002). "Complete mutation analysis panel of the 39 human HOX genes". Teratology. ج. 65 ع. 2: 50–62. DOI:10.1002/tera.10009. PMID:11857506.
Chau YM، Pando S، Taylor HS (يونيو 2002). "HOXA11 silencing and endogenous HOXA11 antisense ribonucleic acid in the uterine endometrium". The Journal of Clinical Endocrinology and Metabolism. ج. 87 ع. 6: 2674–80. DOI:10.1210/jc.87.6.2674. PMID:12050232.