Mendelian inheritance in man and its online version, OMIM

被引：515
作者：
McKusick, Victor A. [1 ]
机构：
[1] Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21218 USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2007年 / 80卷 / 04期
关键词：
D O I：
10.1086/514346
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：588 / 604
页数：17
相关论文
共 81 条
[1]   Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans [J].
Aitman, TJ ;
Dong, R ;
Vyse, TJ ;
Norsworthy, PJ ;
Johnson, MD ;
Smith, J ;
Mangion, J ;
Roberton-Lowe, C ;
Marshall, AJ ;
Petretto, E ;
Hodges, MD ;
Bhangal, G ;
Patel, SG ;
Sheehan-Rooney, K ;
Duda, M ;
Cook, PR ;
Evans, DJ ;
Domin, J ;
Flint, J ;
Boyle, JJ ;
Pusey, CD ;
Cook, HT .
NATURE, 2006, 439 (7078) :851-855
[2]  
[Anonymous], 1992, MENDELIAN INHERITANC
[3]   Opinion - Mendelian disorders deserve more attention [J].
Antonarakis, SE ;
Beckmann, JS .
NATURE REVIEWS GENETICS, 2006, 7 (04) :277-282
[4]   OMIM passes the 1,000-disease-gene mark [J].
Antonarakis, SE ;
McKusick, VA .
NATURE GENETICS, 2000, 25 (01) :11-11
[5]  
Antonarakis SE, 1998, HUM MUTAT, V11, P1
[6]   FURTHER EVIDENCE FOR LOCATION OF THE SPHEROCYTOSIS GENE ON CHROMOSOME-8 [J].
BASS, EB ;
SMITH, SW ;
STEVENSON, RE ;
ROSSE, WF .
ANNALS OF INTERNAL MEDICINE, 1983, 99 (02) :192-193
[7]   The common variants/multiple disease hypothesis of common complex genetic disorders [J].
Becker, KG .
MEDICAL HYPOTHESES, 2004, 62 (02) :309-317
[8]  
BERGSMA D, 1969, Birth Defects Original Article Series, V5, P1
[9]  
BUCKLE VJ, 1984, CLIN GENET, V26, P1, DOI 10.1111/j.1399-0004.1984.tb00780.x
[10]  
Burchfield R., 1991, UNLOCKING ENGLISH LA
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