Online Mendelian Inheritance in Man (Simple English Wikipedia)

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

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archive.org

McKusick, VA (1998). Mendelian inheritance in man: a catalog of human genes and genetic disorders. Baltimore, Maryland: Johns Hopkins University Press. ISBN 978-0-8018-5742-3.

doi.org

Hamosh A.; Scott A.; Amberger J.; Bocchini C.; McKusick V. (2004). "Online Mendelian Inheritance in Man (OMIM): a knowledgebase of human genes and genetic disorders". Nucleic Acids Research. 33 (Database issue): D514 – D517. doi:10.1093/nar/gki033. PMC 539987. PMID 15608251.
McKusick V.; Amberger J. (1993). "The morbid anatomy of the human genome: chromosomal location of mutations causing disease". Journal of Medical Genetics. 30 (1): 1–26. doi:10.1136/jmg.30.1.1. PMC 1016229. PMID 8423603.
Tolmie J.; et al. (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.

nih.gov

ncbi.nlm.nih.gov

Hamosh A.; Scott A.; Amberger J.; Bocchini C.; McKusick V. (2004). "Online Mendelian Inheritance in Man (OMIM): a knowledgebase of human genes and genetic disorders". Nucleic Acids Research. 33 (Database issue): D514 – D517. doi:10.1093/nar/gki033. PMC 539987. PMID 15608251.
"National Center for Biotechnology Information". Retrieved 2011-04-20.
McKusick V.; Amberger J. (1993). "The morbid anatomy of the human genome: chromosomal location of mutations causing disease". Journal of Medical Genetics. 30 (1): 1–26. doi:10.1136/jmg.30.1.1. PMC 1016229. PMID 8423603.
Tolmie J.; et al. (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.

pubmed.ncbi.nlm.nih.gov

Hamosh A.; Scott A.; Amberger J.; Bocchini C.; McKusick V. (2004). "Online Mendelian Inheritance in Man (OMIM): a knowledgebase of human genes and genetic disorders". Nucleic Acids Research. 33 (Database issue): D514 – D517. doi:10.1093/nar/gki033. PMC 539987. PMID 15608251.
McKusick V.; Amberger J. (1993). "The morbid anatomy of the human genome: chromosomal location of mutations causing disease". Journal of Medical Genetics. 30 (1): 1–26. doi:10.1136/jmg.30.1.1. PMC 1016229. PMID 8423603.
Tolmie J.; et al. (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.org

"OMIM Entry Statistics". Online Mendelian Inheritance in Man. Baltimore, MD: McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University. 2015. Retrieved 23 July 2015.
"OMIM Help". Retrieved 2011-04-20.
"OMIM Help". Retrieved 2011-04-18.