McKusick, V. A. (2007). »Mendelian Inheritance in Man and its online version, OMIM«. Am. J. Hum. Genet. Zv. 80, št. 4. str. 588–604. doi:10.1086/514346. PMC1852721. PMID17357067.
Amberger, J.; Bocchini, C.; Hamosh, A. (2011). »A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®)«. Hum. Mutat. Zv. 32, št. 5. str. 564–7. doi:10.1002/humu.21466. PMID21472891.
Amberger, J.S.; Bocchini, C.A.; Schiettecatte, F.; Scott, A.F.; Hamosh, A. (2015). »OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders«. Nucleic Acids Res. Zv. 43, št. Database issue. str. D789-98. doi:10.1093/nar/gku1205. PMC4383985. PMID25428349.
Gitomer, W.; Pak, C. (1996). »Recent advances in the biochemical and molecular biological basis of cystinuria«. The Journal of Urology. Zv. 156, št. 6. str. 1907–1912. doi:10.1016/S0022-5347(01)65389-8. PMID8911353.
Tolmie, J.; Shillito, P.; Hughes-Benzie, R.; Stephenson, J. (1995). »The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis)«. Journal of Medical Genetics. Zv. 32, št. 11. str. 881–884. doi:10.1136/jmg.32.11.881. PMC1051740. PMID8592332.
nih.gov
pubmed.ncbi.nlm.nih.gov
McKusick, V. A. (2007). »Mendelian Inheritance in Man and its online version, OMIM«. Am. J. Hum. Genet. Zv. 80, št. 4. str. 588–604. doi:10.1086/514346. PMC1852721. PMID17357067.
Amberger, J.; Bocchini, C.; Hamosh, A. (2011). »A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®)«. Hum. Mutat. Zv. 32, št. 5. str. 564–7. doi:10.1002/humu.21466. PMID21472891.
Amberger, J.S.; Bocchini, C.A.; Schiettecatte, F.; Scott, A.F.; Hamosh, A. (2015). »OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders«. Nucleic Acids Res. Zv. 43, št. Database issue. str. D789-98. doi:10.1093/nar/gku1205. PMC4383985. PMID25428349.
Gitomer, W.; Pak, C. (1996). »Recent advances in the biochemical and molecular biological basis of cystinuria«. The Journal of Urology. Zv. 156, št. 6. str. 1907–1912. doi:10.1016/S0022-5347(01)65389-8. PMID8911353.
Tolmie, J.; Shillito, P.; Hughes-Benzie, R.; Stephenson, J. (1995). »The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis)«. Journal of Medical Genetics. Zv. 32, št. 11. str. 881–884. doi:10.1136/jmg.32.11.881. PMC1051740. PMID8592332.
ncbi.nlm.nih.gov
McKusick, V. A. (2007). »Mendelian Inheritance in Man and its online version, OMIM«. Am. J. Hum. Genet. Zv. 80, št. 4. str. 588–604. doi:10.1086/514346. PMC1852721. PMID17357067.
Amberger, J.S.; Bocchini, C.A.; Schiettecatte, F.; Scott, A.F.; Hamosh, A. (2015). »OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders«. Nucleic Acids Res. Zv. 43, št. Database issue. str. D789-98. doi:10.1093/nar/gku1205. PMC4383985. PMID25428349.
Tolmie, J.; Shillito, P.; Hughes-Benzie, R.; Stephenson, J. (1995). »The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis)«. Journal of Medical Genetics. Zv. 32, št. 11. str. 881–884. doi:10.1136/jmg.32.11.881. PMC1051740. PMID8592332.
omim.org
»OMIM Entry Statistics«. Online Mendelian Inheritance in Man. Baltimore, MD: McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University. 2017. Pridobljeno 12. februarja 2017.
»FAQ, §1.2«. Online Mendelian Inheritance in Man. Baltimore, MD: McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University. 2015. Pridobljeno 23. julija 2015.
