451 related articles for article (PubMed ID: 10612823)
1. Online Mendelian Inheritance in Man (OMIM).
Hamosh A; Scott AF; Amberger J; Valle D; McKusick VA
Hum Mutat; 2000; 15(1):57-61. PubMed ID: 10612823
[TBL] [Abstract][Full Text] [Related]
2. Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders.
Hamosh A; Scott AF; Amberger J; Bocchini C; Valle D; McKusick VA
Nucleic Acids Res; 2002 Jan; 30(1):52-5. PubMed ID: 11752252
[TBL] [Abstract][Full Text] [Related]
3. Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders.
Hamosh A; Scott AF; Amberger JS; Bocchini CA; McKusick VA
Nucleic Acids Res; 2005 Jan; 33(Database issue):D514-7. PubMed ID: 15608251
[TBL] [Abstract][Full Text] [Related]
4. [Application of Online Mendelian Inheritance in Man to medical genetics].
Hu YA; Cui YX
Zhonghua Nan Ke Xue; 2011 Jul; 17(7):639-43. PubMed ID: 21823350
[TBL] [Abstract][Full Text] [Related]
5. Database resources of the National Center for Biotechnology Information: update.
Wheeler DL; Church DM; Edgar R; Federhen S; Helmberg W; Madden TL; Pontius JU; Schuler GD; Schriml LM; Sequeira E; Suzek TO; Tatusova TA; Wagner L
Nucleic Acids Res; 2004 Jan; 32(Database issue):D35-40. PubMed ID: 14681353
[TBL] [Abstract][Full Text] [Related]
6. Using OMIM (On-line Mendelian Inheritance in Man) as an expert system in medical genetics.
Schorderet DF
Am J Med Genet; 1991 Jun; 39(3):278-84. PubMed ID: 1867277
[TBL] [Abstract][Full Text] [Related]
7. Human gene mutation database-a biomedical information and research resource.
Krawczak M; Ball EV; Fenton I; Stenson PD; Abeysinghe S; Thomas N; Cooper DN
Hum Mutat; 2000; 15(1):45-51. PubMed ID: 10612821
[TBL] [Abstract][Full Text] [Related]
8. NCBI genetic resources supporting immunogenetic research.
Feolo M; Helmberg W; Sherry S; Maglott DR
Rev Immunogenet; 2000; 2(4):461-7. PubMed ID: 12361089
[TBL] [Abstract][Full Text] [Related]
9. CGMIM: automated text-mining of Online Mendelian Inheritance in Man (OMIM) to identify genetically-associated cancers and candidate genes.
Bajdik CD; Kuo B; Rusaw S; Jones S; Brooks-Wilson A
BMC Bioinformatics; 2005 Mar; 6():78. PubMed ID: 15796777
[TBL] [Abstract][Full Text] [Related]
10. OMIA (Online Mendelian Inheritance in Animals): an enhanced platform and integration into the Entrez search interface at NCBI.
Lenffer J; Nicholas FW; Castle K; Rao A; Gregory S; Poidinger M; Mailman MD; Ranganathan S
Nucleic Acids Res; 2006 Jan; 34(Database issue):D599-601. PubMed ID: 16381939
[TBL] [Abstract][Full Text] [Related]
11. Genetics of growth retardation.
Phillips JA
J Pediatr Endocrinol Metab; 2004 Mar; 17 Suppl 3():385-99. PubMed ID: 15134299
[TBL] [Abstract][Full Text] [Related]
12. A new face and new challenges for Online Mendelian Inheritance in Man (OMIMĀ®).
Amberger J; Bocchini C; Hamosh A
Hum Mutat; 2011 May; 32(5):564-7. PubMed ID: 21472891
[TBL] [Abstract][Full Text] [Related]
13. Internet resources for the clinical geneticist.
Ouellette F
Clin Genet; 1999 Sep; 56(3):179-85. PubMed ID: 10563474
[TBL] [Abstract][Full Text] [Related]
14. Online Mendelian Inheritance in Man (OMIMĀ®): Victor McKusick's magnum opus.
Hamosh A; Amberger JS; Bocchini C; Scott AF; Rasmussen SA
Am J Med Genet A; 2021 Nov; 185(11):3259-3265. PubMed ID: 34169650
[TBL] [Abstract][Full Text] [Related]
15. McKusick's Online Mendelian Inheritance in Man (OMIM).
Amberger J; Bocchini CA; Scott AF; Hamosh A
Nucleic Acids Res; 2009 Jan; 37(Database issue):D793-6. PubMed ID: 18842627
[TBL] [Abstract][Full Text] [Related]
16. The cypriot and Iranian National Mutation Frequency Databases.
Kleanthous M; Patsalis PC; Drousiotou A; Motazacker M; Christodoulou K; Cariolou M; Baysal E; Khrizi K; Moghimi B; Pourfarzad F; van Baal S; Deltas C; Najmabadi H; Patrinos GP
Hum Mutat; 2006 Jun; 27(6):598-9. PubMed ID: 16705699
[TBL] [Abstract][Full Text] [Related]
17. Victor Almon McKusick: In the footsteps of Mendel and Osler.
Francomano CA
Am J Med Genet A; 2021 Nov; 185(11):3193-3201. PubMed ID: 34463023
[TBL] [Abstract][Full Text] [Related]
18. Contribution of Mendelian disorders to common chronic disease: opportunities for recognition, intervention, and prevention.
Scheuner MT; Yoon PW; Khoury MJ
Am J Med Genet C Semin Med Genet; 2004 Feb; 125C(1):50-65. PubMed ID: 14755434
[TBL] [Abstract][Full Text] [Related]
19. Singapore Human Mutation/Polymorphism Database: a country-specific database for mutations and polymorphisms in inherited disorders and candidate gene association studies.
Tan EC; Loh M; Chuon D; Lim YP
Hum Mutat; 2006 Mar; 27(3):232-5. PubMed ID: 16429432
[TBL] [Abstract][Full Text] [Related]
20. Hellenic National Mutation database: a prototype database for mutations leading to inherited disorders in the Hellenic population.
Patrinos GP; van Baal S; Petersen MB; Papadakis MN
Hum Mutat; 2005 Apr; 25(4):327-33. PubMed ID: 15776445
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]