Online Mendelian Inheritance in Man (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Online Mendelian Inheritance in Man" in English language version.

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McKusick, V. A. (2007). "Mendelian Inheritance in Man and its online version, OMIM". Am. J. Hum. Genet. 80 (4): 588–604. doi:10.1086/514346. PMC 1852721. PMID 17357067.
Amberger, J.; Bocchini, C.; Hamosh, A. (2011). "A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®)". Hum. Mutat. 32 (5): 564–7. doi:10.1002/humu.21466. PMID 21472891. S2CID 39087815.
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. 43 (Database issue): D789-98. doi:10.1093/nar/gku1205. PMC 4383985. PMID 25428349.
Gitomer, W.; Pak, C. (1996). "Recent advances in the biochemical and molecular biological basis of cystinuria". The Journal of Urology. 156 (6): 1907–1912. doi:10.1016/S0022-5347(01)65389-8. PMID 8911353.
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. 32 (11): 881–884. doi:10.1136/jmg.32.11.881. PMC 1051740. PMID 8592332.

McKusick, V. A. (2007). "Mendelian Inheritance in Man and its online version, OMIM". Am. J. Hum. Genet. 80 (4): 588–604. doi:10.1086/514346. PMC 1852721. PMID 17357067.
Amberger, J.; Bocchini, C.; Hamosh, A. (2011). "A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®)". Hum. Mutat. 32 (5): 564–7. doi:10.1002/humu.21466. PMID 21472891. S2CID 39087815.
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. 43 (Database issue): D789-98. doi:10.1093/nar/gku1205. PMC 4383985. PMID 25428349.
Gitomer, W.; Pak, C. (1996). "Recent advances in the biochemical and molecular biological basis of cystinuria". The Journal of Urology. 156 (6): 1907–1912. doi:10.1016/S0022-5347(01)65389-8. PMID 8911353.
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. 32 (11): 881–884. doi:10.1136/jmg.32.11.881. PMC 1051740. PMID 8592332.

"OMIM Entry Statistics". Online Mendelian Inheritance in Man. Baltimore, MD: McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University. 2019. Retrieved 28 June 2019.
"FAQ, §1.2". Online Mendelian Inheritance in Man. Baltimore, MD: McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University. 2015. Retrieved 23 July 2015.
"Hemoglobin beta locus or HBB (141900): Allelic variants". Online Mendelian Inheritance in Man. Baltimore, MD: McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University. 2015. Retrieved 23 July 2015.
"FAQ, §1.3". Online Mendelian Inheritance in Man. Baltimore, MD: McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University. 2015. Retrieved 23 July 2015.

Amberger, J.; Bocchini, C.; Hamosh, A. (2011). "A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®)". Hum. Mutat. 32 (5): 564–7. doi:10.1002/humu.21466. PMID 21472891. S2CID 39087815.